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BioCol

FDA UDI

Class U (US FDA UDI)

by Southwest Technologies, Inc.

Identity

Trade Name
BioCol FDA UDI
Generic Name
Animal-derived wound matrix dressing FDA UDI
Device Name
1 gram Collagen Powder FDA UDI
Model / Reference
AWC01 FDA UDI
Description
1 gram Collagen Powder FDA UDI

Identifiers

Catalog Number
8-050-001 FDA UDI
Primary DI / UDI-DI
00745713186015 FDA UDI
510(k) Number
K030774 FDA UDI
FDA Product Code
KGN FDA UDI
GMDN Term
Animal-derived wound matrix dressing FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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: Animal-derived wound matrix dressing

BioCol by Southwest Technologies, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Animal-derived wound matrix dressing.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 82f031fd-8942-40d0-89d4-ee25401d5f9d 37 fields · synced Jun 1, 2026