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Disposable Waste Collector

FDA UDI

Class I (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name
DISPOSABLE WASTE COLLECTOR FDA UDI
Generic Name
Contaminated waste container FDA UDI
Model / Reference
907209 FDA UDI

Identifiers

Catalog Number
907209 FDA UDI
Primary DI / UDI-DI
00880304408869 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Contaminated waste container FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Contaminated waste container

Disposable Waste Collector by Biomet Orthopedics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Contaminated waste container.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 05a7b7c9-c465-4b09-9bea-99fa13a4e981 35 fields · synced Jun 6, 2026