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CevOss - CITAGENIX

FDA UDI

Class II (US FDA UDI)

by Odontit S.a.

Identity

Trade Name
CevOss - CITAGENIX FDA UDI
Generic Name
Dental bone matrix implant, animal-derived FDA UDI
Device Name
CevOss .5cc Bovine bone graft .25-1mm vial FDA UDI
Model / Reference
CEV02-05 FDA UDI
Description
CevOss .5cc Bovine bone graft .25-1mm vial FDA UDI

Identifiers

Primary DI / UDI-DI
D914CEV0205 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

Category: Dental bone matrix implant, animal-derived

CevOss - CITAGENIX by Odontit S.a. — 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

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Manufacturer

Manufacturer
Odontit S.a.

Sources (1)

  • FDA UDI a6072dff-40f4-4034-8cfa-2e0ed0e3d571 34 fields · synced May 29, 2026