Notified body · Verified from EUDAMED
We show only what EUDAMED publishes. EUDAMED is still being populated — the absence of a certificate here does not mean none exists. Every figure links back to the official record so you can verify it yourself.
Lens 06 · Published fees
What it means: notified bodies must make their standard fees publicly available (Article 50 MDR, Article 46 IVDR). The European Commission keeps an index of the fee lists it has been given.
| Regulation | Fee list |
|---|---|
| MDR | DNV MEDCERT Certification Services ↗Web page |
Links come from the European Commission's index of notified-body fee lists. We link out to each body's own site — we do not host the documents, read the amounts, or check that a link still resolves. Index retrieved Jul 14, 2026. Open the source index →
Lens 02 · From the certificates
Device-group families derived from the scope text of this body's issued certificates (often legacy nomenclature) — not the official NANDO designation scope.
Read from the certificate scope text, which is messy free-text and skews to legacy nomenclature. We render only the code families actually present rather than imply a modern device-group breakdown that isn't recorded.
These families are read from the issued certificates' scope text (often legacy nomenclature), not the official NANDO scope of designation.
MDA — Active devices
MDN — Non-active devices
MDS — Devices with specific characteristics (horizontal)
MDT — Devices using specific technologies / processes (horizontal)
IVR — IVD devices, base group (design / intended purpose)
IVS — IVDs with specific characteristics
IVT — IVDs using specific technologies
IVP — Specific examination-procedure knowledge
IVD — Specific laboratory / clinical-discipline knowledge
Source: Commission Implementing Reg (EU) 2017/2185; MDCG 2019-14 (MDR) / 2021-14 (IVDR).
Lens 03 · Certificates
What it means: most of this body's certificates are live; a small share have ended or had adverse action.
| Status | Count | Distribution | Share |
|---|---|---|---|
| Issued | 83 | 66.4% | |
| Supplemented | 28 | 22.4% | |
| Amended | 8 | 6.4% | |
| Reissued | 4 | 3.2% | |
| Withdrawn | 1 | 0.8% | |
| Cancelled | 1 | 0.8% | |
| Total recorded | 125 | 100% |
+ 2 expired (derived from the expiry date, not a EUDAMED status).
New certificates per year — the curve of EUDAMED adoption.
Lens 04 · What it certifies
What it means: higher classes (MDR III, IVDR D) carry the strictest scrutiny — a window into how high-stakes this body's work runs.
| Framework | Class | Certs | Distribution |
|---|---|---|---|
| MDR | Class I | 21 | |
| Class IIa | 59 | ||
| Class IIb | 46 | ||
| Class III | 45 |
A certificate may cover several risk classes; these counts are not additive.
Common questions
Based on EUDAMED data, DNV MEDCERT GmbH (NB 0482) has issued 125 certificates: 125 under the EU MDR and 0 under the EU IVDR. EUDAMED is still being populated, so this is a lower bound, not a complete history.
Across its issued certificates it has covered MDR Class I, IIa, IIb and III devices and IVDR Class A, B, C and D devices, including the highest-risk MDR Class III and IVDR Class D.
Yes. This body is designated under the EU IVDR (2017/746) and the EU MDR (2017/745), plus the legacy AIMDD, MDD and IVDD directives. Its official scope of designation is published on NANDO ↗.
In one line
DNV MEDCERT GmbH (notified body 0482) is a Germany notified body designated under the EU MDR and IVDR. Based on EUDAMED data, it has issued 125 certificates (125 MDR, 0 IVDR) to 95 manufacturers across 11 countries.
Lens 05 · Who relies on it
What it means: 95 distinct manufacturers across 11 countries rely on this body.
| Manufacturer | Country | Certs |
|---|---|---|
| Waldemar Link GmbH & Co. KG | 🇩🇪 DE | 15 |
| TERUMO EUROPE N.V. | 🇧🇪 BE | 3 |
| BIOTRONIK SE & Co. KG | 🇩🇪 DE | 3 |
| Aesculap AG | 🇩🇪 DE | 3 |
| Luciole Medical AG | 🇨🇭 CH | 2 |
| Neuromedex GmbH | 🇩🇪 DE | 2 |
| PlantTec Medical GmbH | 🇩🇪 DE | 2 |
| UROMED Kurt Drews KG | 🇩🇪 DE | 2 |
| 🇩🇪 DE | 2 | |
| 🇩🇪 DE | 2 | |
| 🇩🇪 DE | 2 | |
| 🇩🇪 DE | 2 | |
| 🇩🇪 DE | 2 | |
| 🇮🇱 IL | 2 | |
| 🇦🇺 AU | 1 | |
| 🇧🇪 BE | 1 | |
| 🇨🇭 CH | 1 | |
| 🇨🇭 CH | 1 | |
| 🇨🇭 CH | 1 | |
| 🇨🇳 CN | 1 |
| Country | Manufacturers | Share |
|---|---|---|
| 🇩🇪 Germany | 64 | |
| 🇨🇳 China | 8 | |
| 🇮🇱 Israel | 7 | |
| 🇨🇭 Switzerland | 4 | |
| 🇳🇱 Netherlands | 3 | |
| 🇺🇸 United States | 3 | |
| 🇧🇪 Belgium | 2 |
Lens 01 · Mandate
The regulations this body is designated under, plus any predecessor directives.
| Regulation | Designation | Authoritative record |
|---|---|---|
| MDR | Active | Verify on NANDO ↗ |
| AIMDD(legacy) | Designated (legacy) | — |
| MDD(legacy) | Designated (legacy) | — |
“Active” means the designation is currently valid in NANDO, the EU’s official register; where NANDO does not confirm an active status we show “Designated” and link out rather than a status we cannot verify. Active status verified on NANDO Jul 20, 2026. Official scope of designation is published on NANDO →
| 🇦🇺 Australia | 1 |
| across 95 manufacturers | 95 | 11 countries total |