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Geistlich Perio-System Combi-Pack

FDA UDI

Class II (US FDA UDI)

by Geistlich Pharma AG

Identity

Trade Name
Geistlich Perio-System Combi-Pack FDA UDI
Generic Name
Dental bone matrix implant, animal-derived FDA UDI
Model / Reference
20147 FDA UDI

Identifiers

Primary DI / UDI-DI
07610221010387 FDA UDI
FDA Product Code
NPM FDA UDI
NPL 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

Yes

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-derivedCollagen dental regeneration membrane

Geistlich Perio-System Combi-Pack by Geistlich Pharma AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Collagen dental regeneration membrane.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Geistlich Pharma AG

Sources (1)

  • FDA UDI dbb023a9-3564-46a3-ae96-daad3d8aa995 32 fields · synced May 30, 2026