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Shaver Interface

FDA UDI

Class I (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name
SHAVER INTERFACE FDA UDI
Generic Name
Arthroscopic irrigation/insufflation system FDA UDI
Model / Reference
906028F FDA UDI

Identifiers

Catalog Number
906028F FDA UDI
Primary DI / UDI-DI
00880304644694 FDA UDI
FDA Product Code
NBH FDA UDI
GMDN Term
Arthroscopic irrigation/insufflation system FDA UDI

Classification

Device Class
Class I 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

Yes

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: Arthroscopic irrigation/insufflation system

Shaver Interface by Biomet Orthopedics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arthroscopic irrigation/insufflation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2c1eb5ff-a3ab-4fd9-acc8-9520630a7161 34 fields · synced Jun 6, 2026