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Optivac Kit, 40 gram single Mix

FDA UDI

Class I (US FDA UDI)

by Biomet, Inc.

Identity

Trade Name
Optivac Kit, 40 gram single Mix FDA UDI
Generic Name
Orthopaedic cement preparation/delivery kit FDA UDI
Model / Reference
417100 FDA UDI

Identifiers

Catalog Number
417100 FDA UDI
Primary DI / UDI-DI
00880304370579 FDA UDI
FDA Product Code
JDZ FDA UDI
GMDN Term
Orthopaedic cement preparation/delivery kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4210 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthopaedic cement preparation/delivery kit

Optivac Kit, 40 gram single Mix by Biomet, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic cement preparation/delivery kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biomet, Inc.

Sources (1)

  • FDA UDI 181fcf37-a9dc-4e6b-8cc1-47f112dc7148 35 fields · synced Jun 6, 2026