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4mm X 9ft. Light Cable

FDA UDI

Class II (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name
4MM X 9FT. LIGHT CABLE FDA UDI
Generic Name
Fibreoptic light cable FDA UDI
Model / Reference
906117 FDA UDI

Identifiers

Catalog Number
906117 FDA UDI
Primary DI / UDI-DI
00880304463912 FDA UDI
510(k) Number
K920800 FDA UDI
FDA Product Code
HRX FDA UDI
GMDN Term
Fibreoptic light cable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.1100 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Fibreoptic light cable

4mm X 9ft. Light Cable by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fibreoptic light cable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ead905d2-fa7f-4cf7-9dfb-4b77506f9826 35 fields · synced May 30, 2026