Identity
- Trade Name
- Ophthalmic trocar FDA UDI
- Generic Name
- Ophthalmic cannula transscleral trocar blade FDA UDI
- Device Name
- A rigid, ophthalmic surgical instrument with a sharp pyramidal or conical point used to puncture the eye to provide access to the interior of the eye for ophthalmic surgery. It is assembled and used together with a compatible cannula, filling its lumen and providing the necessary sharp point, thereby facilitating the introduction of this assembly. The trocar is withdrawn after puncturing, providing a working channel into the interior of the eye. It is typically available for use with an ophthalmic cannulation set. This is a reusable device. FDA UDI
- Model / Reference
- RETILOCK® 23G NON VALVED SELF-RETAINING TROCAR FDA UDI
- Description
- A rigid, ophthalmic surgical instrument with a sharp pyramidal or conical point used to puncture the eye to provide access to the interior of the eye for ophthalmic surgery. It is assembled and used together with a compatible cannula, filling its lumen and providing the necessary sharp point, thereby facilitating the introduction of this assembly. The trocar is withdrawn after puncturing, providing a working channel into the interior of the eye. It is typically available for use with an ophthalmic cannulation set. This is a reusable device. FDA UDI
Identifiers
- Catalog Number
- S9.7000.23 FDA UDI
- Primary DI / UDI-DI
- 03760087123876 FDA UDI
- FDA Product Code
- NGY FDA UDI
- GMDN Term
- Ophthalmic cannula transscleral trocar blade 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
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Ethylene Oxide FDA UDI
Dimensions & Sizes
- Size
- Needle Gauge — 23 Gauge FDA UDI
Category: Ophthalmic cannula transscleral trocar blade
Ophthalmic trocar by Fci S A S Fci 20 22 — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Ophthalmic cannula transscleral trocar blade.
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- Ophthalmic trocar — FCI S A S FCI 20 22 · Class I
- Ophthalmic trocar — FCI S A S FCI 20 22 · Class I
- Ophthalmic trocar — FCI S A S FCI 20 22 · Class I
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
- Manufacturer
- Fci S A S Fci 20 22
Sources (1)
- FDA UDI 200a1898-43e5-45a2-9d87-ebdf65ad1043 36 fields · synced May 30, 2026