Identity
- Trade Name
- Duckworth & Kent FDA UDI
- Generic Name
- Manual intraocular lens injector, reusable FDA UDI
- Device Name
- IOL Injector EUDAMEDFDA UDI
- Model / Reference
- DK7797-2 EUDAMEDFDA UDI
- Description
- IOL Injector FDA UDI
Identifiers
- Catalog Number
- DK7797-2 FDA UDI
- Primary DI / UDI-DI
- 05055313817222 EUDAMEDFDA UDI
- Basic UDI-DI
- B-05055313817222 EUDAMED
- 510(k) Number
- K072985 FDA UDI
- FDA Product Code
- KYB FDA UDI
- EMDN Code
- L1709 OCULAR IMPLANT INSTRUMENTS NOT INCLUDED IN OTHER CLASSES, REUSABLE EUDAMED
- GMDN Term
- Manual intraocular lens injector, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 886.4300 FDA UDI
- Market of Registration
- Belgium 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
No
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
IOL Injector 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-05055313817222 | 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 6b9d0ce5-4096-4628-afaf-25ff4dcb6086 61 fields · synced Jul 11, 2026
- FDA UDI 8747f556-a61f-4ea0-9827-11defa6abda1 36 fields · synced May 29, 2026