Identity
- Trade Name
- Duckworth & Kent FDA UDI
- Generic Name
- Ophthalmic surgical device handling forceps, reusable FDA UDI
- Device Name
- Tying Forceps EUDAMEDFDA UDI
- Model / Reference
- 2-520E EUDAMEDFDA UDI
- Description
- Tying Forceps FDA UDI
Identifiers
- Catalog Number
- 2-520E FDA UDI
- Primary DI / UDI-DI
- 05055313832119 EUDAMEDFDA UDI
- Basic UDI-DI
- B-05055313832119 EUDAMED
- FDA Product Code
- HNR FDA UDI
- EMDN Code
- L170203 FORCEPS FOR HANDLING DEVICES FOR OPHTHALMIC USE, REUSABLE EUDAMED
- GMDN Term
- Ophthalmic surgical device handling forceps, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 886.4350 FDA UDI
- Market of Registration
- Slovakia 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
Tying 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-05055313832119 | 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 ad892ca0-dd79-4446-9308-718099db6f3f 61 fields · synced Sep 17, 2026
- FDA UDI 7d2eaff4-1bb3-4266-9aec-5f3871cb7205 35 fields · synced May 29, 2026