Identity
- Trade Name
- Alcon FDA UDI
- Generic Name
- Fibreoptic operating light system FDA UDI
- Device Name
- 27+DS Wide Angle Light Probe FDA UDI
- Model / Reference
- 00380650002532 FDA UDI
- Description
- 27+DS Wide Angle Light Probe FDA UDI
Identifiers
- Catalog Number
- 8065000253 FDA UDI
- Primary DI / UDI-DI
- 00380650002532 FDA UDI
- FDA Product Code
- MPA FDA UDI
- GMDN Term
- Fibreoptic operating light system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 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: Fibreoptic operating light system
Alcon by Alcon Laboratories, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Fibreoptic operating light system.
- LUCENT — SPINAL ELEMENTS, INC. · Class II
- LUCENT — SPINAL ELEMENTS, INC. · Class II
- LUCENT — SPINAL ELEMENTS, INC. · Class II
- LUCENT — SPINAL ELEMENTS, INC. · Class II
- Endocraft LLC — Endocraft LLC · Class I
- LUCENT — SPINAL ELEMENTS, INC. · Class II
- PhotonGuide Adapt — Stryker Corp. · Class II
- VARIANT — CAMBER SPINE TECHNOLOGIES · 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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Alcon Laboratories, Inc.
Sources (1)
- FDA UDI ae6b8539-1d71-41c5-8a1d-b5a444aff541 35 fields · synced May 29, 2026