Identity
- Trade Name
- Synergetics FDA UDI
- Generic Name
- Ophthalmic fibreoptic light instrument, single-use FDA UDI
- Device Name
- 25ga Aspirating Endo Illuminator FDA UDI
- Model / Reference
- 56.24.25P FDA UDI
- Description
- 25ga Aspirating Endo Illuminator FDA UDI
Identifiers
- Catalog Number
- 56.24.25P FDA UDI
- Primary DI / UDI-DI
- 20841305107391 FDA UDI
- FDA Product Code
- HQB FDA UDI
- GMDN Term
- Ophthalmic fibreoptic light instrument, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.4690 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Ophthalmic fibreoptic light instrument, single-use
Synergetics by Synergetics Usa, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Ophthalmic fibreoptic light instrument, single-use.
- Disposable Chandelier fiber (one fiber) with Photon connector and guidance needl — D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. · Class II
- VitreQ — Vitreq B.V. · Class II
- 20ga Curved Laser Probe, Quantel — KATALYST SURGICAL, LLC · Class II
- 27ga Stiff MultiFlex Extendable Laser Probe, Quantel Connector — KATALYST SURGICAL, LLC · Class II
- 27ga Stiff MultiFlex Laser Probe, Alcon Connector — KATALYST SURGICAL, LLC · Class II
- VitreQ — Vitreq B.V. · Class II
- 23ga Straight Laser Probe, Quantel — KATALYST SURGICAL, LLC · Class II
- TotalView Endoillumination Probe, including illuminated scleral depressor.(27 ga — D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. · Class II
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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Synergetics Usa, Inc.
Sources (1)
- FDA UDI cda42aba-cc64-43f3-bb9b-81b126066c2e 35 fields · synced Jun 1, 2026