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Reusable Two step cannula system.(23 gauge / 0.6 mm)
FDA UDIClass I (US FDA UDI)
by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
Identity
- Trade Name
- Reusable Two step cannula system.(23 gauge / 0.6 mm) FDA UDI
- Generic Name
- Ophthalmic cannulation set, reusable FDA UDI
- Model / Reference
- 1272.E06 FDA UDI
Identifiers
- Catalog Number
- 1272.E06 FDA UDI
- Primary DI / UDI-DI
- 08717872002408 FDA UDI
- FDA Product Code
- NGY FDA UDI
- GMDN Term
- Ophthalmic cannulation set, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4350 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Ophthalmic cannulation set, reusable
Reusable Two step cannula system.(23 gauge / 0.6 mm) by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. — Class I — FDA UDI — listed in FDA GUDID
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
Sources (1)
- FDA UDI 1a12be12-a6c5-4c4f-abdd-bd91423407cd 33 fields · synced May 30, 2026