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Agc V2 Millennium Instrument

FDA UDI

Class I (US FDA UDI)

by Biomet Uk Ltd

Identity

Trade Name
AGC V2 MILLENNIUM INSTRUMENT FDA UDI
Generic Name
Knee femur prosthesis trial, reusable FDA UDI
Model / Reference
32-468446 FDA UDI

Identifiers

Catalog Number
32-468446 FDA UDI
Primary DI / UDI-DI
05019279496716 FDA UDI
FDA Product Code
HWT FDA UDI
GMDN Term
Knee femur prosthesis trial, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4800 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: Knee femur prosthesis trial, reusable

Agc V2 Millennium Instrument by Biomet Uk Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Knee femur prosthesis trial, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biomet Uk Ltd

Sources (1)

  • FDA UDI 681bac4e-fd30-4725-b840-66b78cb9afa4 35 fields · synced May 31, 2026