← Back to catalogue

Geistlich Bio-Oss Collagen®

FDA UDI

Class II (US FDA UDI)

by Geistlich Pharma AG

Identity

Trade Name
Geistlich Bio-Oss Collagen® FDA UDI
Generic Name
Dental bone matrix implant, animal-derived FDA UDI
Model / Reference
500413 FDA UDI

Identifiers

Primary DI / UDI-DI
07610221012510 FDA UDI
FDA Product Code
NPM FDA UDI
GMDN Term
Dental bone matrix implant, animal-derived FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3930 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

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Weight — 50 Milligram FDA UDI

Category: Dental bone matrix implant, animal-derived

Geistlich Bio-Oss Collagen® by Geistlich Pharma AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental bone matrix implant, animal-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
Geistlich Pharma AG

Sources (1)

  • FDA UDI 83a6df86-219b-4b45-844d-4346d6895cc1 33 fields · synced May 30, 2026