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Avitene

FDA UDI

Class III (US FDA UDI)

by Davol Inc.

Identity

Trade Name
Avitene FDA UDI
Generic Name
Collagen haemostatic agent, non-antimicrobial FDA UDI
Device Name
Syringe Avitene Microfibrillar Collagen Hemostat FDA UDI
Model / Reference
1010340 FDA UDI
Description
Syringe Avitene Microfibrillar Collagen Hemostat FDA UDI

Identifiers

Catalog Number
1010340 FDA UDI
Primary DI / UDI-DI
00801741010507 FDA UDI
FDA Product Code
LMF FDA UDI
GMDN Term
Collagen haemostatic agent, non-antimicrobial FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
878.4490 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 — 1 Gram FDA UDI

Category: Collagen haemostatic agent, non-antimicrobial

Avitene by Davol Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Collagen haemostatic agent, non-antimicrobial.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Davol Inc.

Sources (1)

  • FDA UDI 69089a63-ab79-443c-a3cb-4a9b2cf642ff 38 fields · synced Jun 1, 2026