Identity
- Trade Name
- VitreQ FDA UDI
- Generic Name
- Ophthalmic laser system beam guide FDA UDI
- Device Name
- 23G 90° Directional Laser Probes, Iridex® Compatible FDA UDI
- Model / Reference
- LP23.I04 FDA UDI
- Description
- 23G 90° Directional Laser Probes, Iridex® Compatible FDA UDI
Identifiers
- Primary DI / UDI-DI
- 88719214222372 FDA UDI
- FDA Product Code
- HQF FDA UDIHQB FDA UDI
- GMDN Term
- Ophthalmic laser system beam guide FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.4390 FDA UDI886.4690 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 laser system beam guide
VitreQ by Vitreq B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Ophthalmic laser system beam guide.
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- Synergetics — SYNERGETICS USA, INC. · Class II
- 23-27G BriteLight™ Angled 45° EndoProbe® Box of 6 — Iridex Corporation · Class II
- OtoProbe™ Long Angled Single — Iridex Corporation · Class II
- Synergetics — SYNERGETICS USA, INC. · Class II
- OtoProbe™ Short Angled Box of 6 — Iridex Corporation · 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 |
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Manufacturer
- Manufacturer
- Vitreq B.V.
Sources (1)
- FDA UDI e56f1284-1aec-461d-8eca-3f5466c2f48d 34 fields · synced May 30, 2026