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Veritas Collagen Matrix

FDA UDI

Class II (US FDA UDI)

by Synovis Life Technologies, Inc.

Identity

Trade Name
VERITAS COLLAGEN MATRIX FDA UDI
Generic Name
Extra-gynaecological surgical mesh, collagen, bioabsorbable, non-antimicrobial FDA UDI
Device Name
Veritas Collagen Matrix is an implantable biologic mesh comprised of noncrosslinked bovine pericardium. Veritas Collagen Matrix bovine pericardium is sourced from cattle less than 30 months of age. FDA UDI
Model / Reference
RM-0304 FDA UDI
Description
Veritas Collagen Matrix is an implantable biologic mesh comprised of noncrosslinked bovine pericardium. Veritas Collagen Matrix bovine pericardium is sourced from cattle less than 30 months of age. FDA UDI

Identifiers

Catalog Number
RM0304BIO FDA UDI
Primary DI / UDI-DI
00085412531090 FDA UDI
FDA Product Code
OWV FDA UDI
FTM FDA UDI
OXB FDA UDI
PAJ FDA UDI
OXE FDA UDI
GMDN Term
Extra-gynaecological surgical mesh, collagen, bioabsorbable, non-antimicrobial FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.3300 FDA UDI
Commercial Distribution
Not 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
MRI Safety
MR Safe FDA UDI

Veritas Collagen Matrix by Synovis Life Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ac62bf5b-2b3f-4eb9-b995-0acb0d00f97a 37 fields · synced Jun 1, 2026