← Back to catalogue

Optium®

FDA UDI

Class II (US FDA UDI)

by Lifenet Health

Identity

Trade Name
Optium® FDA UDI
Generic Name
Bone matrix implant, human-derived FDA UDI
Device Name
Optium DBM Gel FDA UDI
Model / Reference
TGEL05 FDA UDI
Description
Optium DBM Gel FDA UDI

Identifiers

Catalog Number
TGEL05 FDA UDI
Primary DI / UDI-DI
00889858450560 FDA UDI
FDA Product Code
MBP FDA UDI
MQV FDA UDI
GMDN Term
Bone matrix implant, human-derived FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3045 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bone matrix implant, human-derived

Optium® by Lifenet Health — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone matrix implant, human-derived.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Lifenet Health

Sources (1)

  • FDA UDI ebebbaf5-d099-48ef-8e48-bdce53c8e810 36 fields · synced Jun 8, 2026