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Endocraft LLC

FDA UDI

Class I (US FDA UDI)

by Endocraft LLC

Identity

Trade Name
Endocraft LLC FDA UDI
Generic Name
Fibreoptic operating light system FDA UDI
Device Name
Fiber optic light carrier for surgical illumination through endoscope. Connects to Light cable. FDA UDI
Model / Reference
UMG105-LCN FDA UDI
Description
Fiber optic light carrier for surgical illumination through endoscope. Connects to Light cable. FDA UDI

Identifiers

Catalog Number
UMG105-LCN FDA UDI
Primary DI / UDI-DI
00860009975187 FDA UDI
FDA Product Code
FEM FDA UDI
GMDN Term
Fibreoptic operating light system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.1500 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

No

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

Category: Fibreoptic operating light system

Endocraft LLC by Endocraft LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fibreoptic operating light system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Endocraft LLC

Sources (1)

  • FDA UDI 9de3c7f2-c6ab-4f41-b40b-c3125e9ca1fc 35 fields · synced May 31, 2026