CECheck The reference for CE marking

CE number lookup: who is Notified Body 0123, 2797 ...?

Last reviewed: October 2026 · Sources listed at the end of this page.

The four-digit number printed after a CE mark identifies a Notified Body. This page lists 74 numbers that are widely seen on products and certificates, each matched to the body that holds or held it, so that you can answer "who is CE 2797?" in a few seconds. For anything that matters, finish the check in NANDO, the Commission's register.

At a glance. This is a selective, unofficial list, dated October 2026. It is not complete, and a number being absent here means nothing. NANDO is the only authoritative record of who is notified, for which legislation and for which products. A number shows that a named body was involved with the product. It does not show that the product is safe, that the certificate is genuine, or that the body was notified for that product. Former UK numbers such as 0086 are flagged: those bodies are not EU-notified.

Search the list

NumberBodyCountryTypical sectors
0035TÜV Rheinland Industrie Service GmbHGermanyATEX; construction products (EN 1090)
0036TÜV SÜD Industrie Service GmbHGermanyPressure equipment
0038LRQA Verification Ltd UK body: not EU-notified.United KingdomPressure equipment (UK regime)
0044TÜV NORD CERT GmbHGermanyMedical devices; ATEX
0050National Standards Authority of Ireland (NSAI)IrelandMedical devices; in vitro diagnostics
0051IMQ Istituto Italiano del Marchio di QualitàItalyMedical devices; machinery
0062Bureau Veritas Services SASFrancePressure equipment; recreational craft
0063Kiwa Nederland B.V.NetherlandsGas appliances; EMC; low voltage
0068MTIC InterCert S.r.l.ItalyMedical devices
0075CTC (Centre Technique Cuir Chaussure Maroquinerie)FrancePPE, including gloves
0080INERISFranceATEX
0082Apave (named as APAVE SA or APAVE SUDEUROPE SAS on declarations)FrancePPE; machinery
0086BSI Assurance UK Ltd UK body: not EU-notified.United KingdomMedical devices and other UK-regime products
0102Physikalisch-Technische Bundesanstalt (PTB)GermanyATEX
0120SGS United Kingdom Ltd UK body: not EU-notified.United KingdomMedical devices (UK regime)
0123TÜV SÜD Product Service GmbHGermanyMedical devices; in vitro diagnostics; machinery; ATEX
0124DEKRA Certification GmbHGermanyMedical devices; in vitro diagnostics
0158DEKRA Testing and Certification GmbHGermanyATEX
0168TÜV SÜD BABT Unlimited UK body: not EU-notified.United KingdomMedical devices (UK regime)
0197TÜV Rheinland LGA Products GmbHGermanyMedical devices; in vitro diagnostics
0297DQS Medizinprodukte GmbHGermanyMedical devices
0318Centro Nacional de Certificación de Productos Sanitarios (CNCps)SpainMedical devices
0321SATRA Technology Centre UK body: not EU-notified.United KingdomPPE (UK regime)
0333AFNOR Certification (AFAQ)FranceMedical devices
0344DEKRA Certification B.V.NetherlandsMedical devices; in vitro diagnostics; ATEX
0400Liftinstituut B.V.NetherlandsLifts and lift safety components
0413Intertek Semko ABSwedenBatteries; older medical device certificates
0425ICIM S.p.A.ItalyMedical devices
0459GMEDFranceMedical devices; in vitro diagnostics
0470Nemko Group ASNorwayRadio equipment; EMC; ATEX; toys
0473AMTAC (Intertek) UK body: not EU-notified.United KingdomFormer medical device body; Intertek said it would close by 1 July 2018
0476Kiwa Cermet ItaliaItalyMachinery; pressure equipment; measuring instruments; medical devices
0477Eurofins Product Testing Italy SrlItalyATEX; lifts; machinery; medical devices; outdoor noise; PPE; pressure equipment
0482DNV MEDCERTGermanyMedical devices
0483mdc medical device certification GmbHGermanyMedical devices; in vitro diagnostics
0537Eurofins Electric & Electronics Finland OyFinlandMedical devices; in vitro diagnostics; ATEX; rail
0539UL International Demko A/SDenmarkATEX
0546CertiqualityItalyMedical devices
0575DNVNorwayMarine equipment; recreational craft
0598SGS Fimko OyFinlandMedical devices; in vitro diagnostics; ATEX
0633Berlin CertGermanyMedical devices
0681Eurofins Product Service GmbHGermanyEMC; radio equipment
0980Eurofins Electrical and Electronic Testing NA, Inc.United StatesRadio equipment
1023Institute for Testing and Certification a.s. (ITC Zlín)CzechiaMedical devices; other acts listed by the body
1258Eurofins Electric & Electronics Product Testing AGSwitzerlandATEX
1282Ente Certificazione Macchine (ECM)ItalyMedical devices; pressure equipment; ATEX
1304Slovenian Institute of Quality and Metrology (SIQ)SloveniaMedical devices
1434Polskie Centrum Badań i Certyfikacji (PCBC)PolandMedical devices
1438CNBOP-PIBPolandConstruction products (System 1)
1622Nemko North America Inc.CanadaRadio equipment
1639SGS Belgium NVBelgiumMedical devices
1912Kiwa Assurance B.V. (formerly listed as Kiwa Dare)NetherlandsMedical devices
1936TÜV Rheinland ItaliaItalyMedical devices
1984Kiwa Türkiye (Kiwa Belgelendirme Hizmetleri A.Ş.)TürkiyeMachinery; construction products; gas appliances; pressure equipment; medical devices; lifts
2051Nemko SpaItalyRadio equipment; EMC
2163Universal CertificationTürkiyePPE, including FFP2 masks
22653EC International a.s.SlovakiaMedical devices; in vitro diagnostics
2274TÜV NORD PolskaPolandMedical devices
2292UDEMTürkiyeMedical devices
2409CE Certiso Kft.HungaryMedical devices
2460DNV Product Assurance ASNorwayMedical devices; ATEX
2571TÜV Rheinland UK Ltd UK body: not EU-notified.United KingdomMedical devices (UK regime)
2696UDEM Adriatic d.o.o.CroatiaMedical devices
2776CML B.V.NetherlandsATEX
2777SATRA Technology Europe LtdIrelandPPE
2797BSI Group The Netherlands B.V.NetherlandsMedical devices; in vitro diagnostics; PPE
2803HTCertCyprusMedical devices
2809FM Approvals Europe LtdIrelandATEX
2813CSA Group Netherlands B.V.NetherlandsATEX
2862Intertek Medical Notified Body ABSwedenMedical devices
2865Eurofins Textile & Footwear Testing SpainSpainPPE
2962QMD Services GmbHAustriaIn vitro diagnostics
3018Sertio Oy (Kiwa Group)FinlandIn vitro diagnostics
3022Scarlet NB B.V.NetherlandsMedical device software and AI

"Typical sectors" shows where we saw the number in use. It is a guide only, not the body's scope of notification, and many bodies cover more. Current status can change at any time: designations are amended, suspended and withdrawn, so a row here is not evidence that a body is notified today. Each entry was matched from the body's own website, a body's own published list, or two independent sources, listed at the end of this page. We did not copy this table from NANDO.

Bodies in Norway, Türkiye, Switzerland, the United States and Canada appear because they are named for specific acts by their own groups or by other sources, through arrangements such as the EEA, the EU-Türkiye customs union and mutual recognition agreements. Their position depends on the act, so check NANDO.

What the number does and does not prove

Under Article R12(3) of Decision No 768/2008/EC, the identification number follows the CE mark when a Notified Body was involved in the production-control phase. The Commission allocates one number per body, even if the body is notified under several acts.

The number tells you:

The number does not tell you:

No number does not by itself mean a problem. Most CE-marked products are self-declared under Module A with no Notified Body, so they carry no number. Some products have a Notified Body certificate for the design only (Module B), with no body involved in production, so no number sits next to the mark even though one appears on the declaration.

How to confirm a number in NANDO

  1. Note the number and the product's legislation. The EU Declaration of Conformity gives both.
  2. Open NANDO or the Single Market Compliance Space and search by notified body number. See our NANDO guide.
  3. Check that the legal entity named matches the one on the certificate. Group companies are notified separately.
  4. Check that the act, the procedure and the product range cover what you hold, and that the notification has not been withdrawn.
  5. To test a specific certificate, ask the body. NANDO lists bodies, not certificates.

Four-digit numbers that are not Notified Body numbers

Some "CE number" searches are for something else. In "Regulation 2023/1230", 1230 is a law number. So is 1542 in Regulation 2023/1542 on batteries and 1009 in Regulation 2019/1009 on fertilising products. Digits in a certificate reference may be a serial number, as in an ATEX reference such as "TÜV 97 ATEX 1172 Q". Model numbers also get mistaken for body numbers. Only a four-digit number placed directly after the CE mark, or named as a Notified Body on the declaration or certificate, is a candidate.

Former UK numbers

UK bodies lost EU notified status at the end of the Brexit transition period and are not EU Notified Bodies. Several numbers live on as UK Approved Body numbers for the UK regime, and they can be read on old stock, old certificates or UKCA documents. A new EU certificate from a UK body is a red flag. BSI, for example, describes 0086 as its UK Approved Body and 2797 as its EU Notified Body in the Netherlands. SATRA uses 0321 for the UK and 2777 for Ireland. A UK Approved Body number beside a UKCA mark is normal. See CE vs UKCA.

Body numbers can also retire within a group. Kiwa Netherlands now uses only 0063, and has said that certificates issued under its older numbers 0620 and 0956 do not need changing. Intertek moved its EU medical work from AMTAC (0473) to Intertek Semko (0413), and Intertek Medical Notified Body (2862) now appears for medical devices.

Numbers we could not confirm

These numbers come up in searches, but we could not match them to a body to our standard, so they are not in the table: 0001, 0048, 0104, 0121, 0246, 0407, 0531, 0596, 0766, 0871, 0957, 1114, 1172, 1242, 1354, 1372, 1674, 2280, 2408, 2528, 2531, 2916, 2927 and 2984. This does not mean that they are invalid. Look them up in NANDO.

Frequently asked questions

Who is Notified Body 0123?

TÜV SÜD Product Service GmbH in Germany. TÜV SÜD itself gives 0123 as its identification number for medical devices, and the number also appears on its machinery and ATEX work. Check the scope in NANDO.

Who is CE 2797?

BSI Group The Netherlands B.V., the Dutch notified body of the BSI group. The BSI UK number, 0086, is now a UK Approved Body number.

Is CE 0086 still valid in the EU?

0086 belongs to BSI Assurance UK Ltd, which is not an EU Notified Body. It remains a UK Approved Body number. A product placed on the EU market today that needs a Notified Body should not rely on a new 0086 certificate. Older units already on the market are a separate matter, so ask the supplier for the paperwork.

Is Notified Body 0482 a UK body?

No. 0482 is DNV MEDCERT in Germany.

Why is my number not in this list?

The list is selective. There are many more Notified Bodies than appear here, and we left out numbers we could not confirm. Search the number in NANDO, which is the only authoritative record.

Does a Notified Body number mean the product is safe?

No. It means that a named body is claimed to have been involved in production control. Safety depends on the product actually conforming, and the manufacturer remains responsible. The number can also be misused, so check it.

Who assigns the number?

The European Commission allocates it when a Member State notifies the body. A body has a single number even if it is notified under several acts.

Sources