Identity
- Trade Name
- Ambler Surgical FDA UDI
- Generic Name
- Fibreoptic light cable FDA UDI
- Device Name
- Fiberoptic light cable, 10' length x 3.5mm bundle diameter, gray sheathing, universal scope / universal light source connectors FDA UDI
- Model / Reference
- Fiberoptic light cable FDA UDI
- Description
- Fiberoptic light cable, 10' length x 3.5mm bundle diameter, gray sheathing, universal scope / universal light source connectors FDA UDI
Identifiers
- Catalog Number
- 40-820 FDA UDI
- Primary DI / UDI-DI
- 00190660100407 FDA UDI
- FDA Product Code
- EQH FDA UDI
- GMDN Term
- Fibreoptic light cable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.4350 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Fibreoptic light cable
A comprehensive surgical device directory, featuring the Ambler Surgical Fiberoptic Light Cable. This product is designed for use in ear, nose, and throat (ENT) procedures, providing high-quality lighting for both visual examination and endoscopic interventions.
Similar devices
Also classified as Fibreoptic light cable.
- JEDMED — JEDMED Instrument Company · Class I
- JEDMED — JEDMED Instrument Company · Class I
- Surgical Direct — SURGICAL DIRECT, INC. · Class II
- Gimmi — Gimmi GmbH · Class II
- ASSI — ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORP. · Class II
- JEDMED — JEDMED Instrument Company · Class I
- Surgical Direct — SURGICAL DIRECT, INC. · Class II
- FENTEX — FENTEX medical GmbH · 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
- Ambler Surgical, LLC
Sources (1)
- FDA UDI c3d0e660-384d-4dd8-b58b-8bd1638cad81 35 fields · synced Jul 5, 2026