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Diamond Knife
EUDAMEDFDA UDIClass I (EU MDR)
Ref ME100Ref A-513Model REIHE: A-200, A-300, A-500, A-800, A-N200, A-NANORef ME420MA
Identity
- Trade Name
- Diamond Knife EUDAMEDMeyco FDA UDI
- Generic Name
- Ophthalmic knife, reusable FDA UDI
- Device Name
- Diamond Knife (Diamantmesser) EUDAMEDdiamond knife for eye surgery FDA UDI
- Model / Reference
- ME100 EUDAMEDFDA UDIME420MA EUDAMEDFDA UDIREIHE: A-200, A-300, A-500, A-800, A-N200, A-NANO EUDAMEDA-513 EUDAMED
- Description
- diamond knife for eye surgery FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05060518820014 EUDAMEDFDA UDI05060518822414 EUDAMEDFDA UDI05060570982460 EUDAMED
- Basic UDI-DI
- B-05060518820014 EUDAMED506057098A-NE EUDAMEDB-05060518822414 EUDAMED
- Direct Marketing DI
- 05060570982460 EUDAMED
- FDA Product Code
- HNN FDA UDI
- EMDN Code
- Q02010101 OPHTHALMIC MICROKNIVES, STRAIGHT EUDAMED
- GMDN Term
- Ophthalmic knife, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 886.4350 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMEDEUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Diamond Knife by Anton Meyer & Co. AG — Class I — MDR, MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | B-05060518820014 | Class I | Active |
| EUDAMED | European Union | CE/MDD | B-05060518820014 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Anton Meyer & Co. AG
- EUDAMED SRN
- CH-MF-000040740
- Authorised Representative
- MDSS GmbH DE-AR-000005430
Sources (5)
- EUDAMED 37d5e032-e898-4f67-947c-23cbb0322d55 61 fields · synced Jul 20, 2026
- FDA UDI 6e8d2a88-4494-4dd9-badf-b8696742f055 34 fields · synced May 30, 2026
- FDA UDI 851992a5-e33e-4548-8b6c-6e38894fd713 34 fields · synced May 30, 2026
- EUDAMED f5f1c05e-2d89-4301-9a3e-89b50c5ccccc 61 fields · synced Jul 13, 2026
- EUDAMED a2e9f39f-58b0-4d30-9a7b-cb3f1f7b5b5d 61 fields · synced Jul 20, 2026