Identity
- Trade Name
- Duckworth & Kent FDA UDI
- Generic Name
- Ophthalmic soft-tissue manipulation forceps, probe-like, reusable FDA UDI
- Device Name
- DMEK Forceps EUDAMEDFDA UDI
- Model / Reference
- 2-838 EUDAMEDFDA UDI
- Description
- DMEK Forceps FDA UDI
Identifiers
- Catalog Number
- 2-838 FDA UDI
- Primary DI / UDI-DI
- 05055313829249 EUDAMEDFDA UDI
- Basic UDI-DI
- B-05055313829249 EUDAMED
- FDA Product Code
- HNR FDA UDI
- EMDN Code
- L170201 OPHTHALMIC GRASPING FORCEPS, REUSABLE EUDAMED
- GMDN Term
- Ophthalmic soft-tissue manipulation forceps, probe-like, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 886.4350 FDA UDI
- Market of Registration
- Spain 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
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
DMEK Forceps by Duckworth & Kent Ltd. — Class I — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-05055313829249 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Duckworth & Kent Ltd.
- EUDAMED SRN
- GB-MF-000002176
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (2)
- EUDAMED d3c18879-cb82-431a-a5fe-d538e32c918b 61 fields · synced Jul 8, 2026
- FDA UDI bdc7a912-19ce-473d-b0b8-fb9b2da79d5a 35 fields · synced May 30, 2026