AccessGUDID - DEVICE: VERITAS COLLAGEN MATRIX (00085412531175)

GUDID

Device Identifier (DI) Information

Brand Name: VERITAS COLLAGEN MATRIX
Version or Model: RM-0618
Commercial Distribution Status: In Commercial Distribution
Catalog Number: RM0618BIO
Company Name: SYNOVIS LIFE TECHNOLOGIES, INC.

Primary DI Number: 00085412531175
Issuing Agency: GS1
Commercial Distribution End Date: September 20, 2026
Device Count: 1
Labeler D-U-N-S® Number*: 017415781 *Terms of Use

Device 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.

Device Characteristics

What MRI safety information does the labeling contain?	MR Safe
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
60907	Extra-gynaecological surgical mesh, collagen, bioabsorbable, non-antimicrobial	A bioabsorbable, implantable material (e.g., flat sheet) made from animal-derived collagen intended for extra-gynaecological, non-dental tissue repair/reinforcement application(s) [e.g., pericardial reinforcement, plastic surgery, abdominal hernia repair]; some types may also be intended for use as a short-term scaffold for tissue regeneration. It is constructed of collagen, which might be cross-linked (e.g., with glutaraldehyde); it does not include antimicrobial agents/materials. Disposable devices associated with implantation may be supplied with the mesh.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
OWV	Mesh, surgical, collagen, diaphragmatic hernia
PAJ	Mesh, surgical, non-synthetic, urogynecologic, for apical vaginal and uterine prolapse, transabdominally placed
OXB	Mesh, surgical, collagen, thoracic, chest wall reconstruction
FTM	Mesh, surgical
OXE	Mesh, surgical, collagen, staple line reinforcement

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Storage Environment Temperature: between 68 and 77 Degrees Fahrenheit
Storage Environment Temperature: between 20 and 25 Degrees Celsius
Special Storage Condition, Specify: Store at a controlled room temperature. Keep away from heat. Do not use if heat indicator is red.

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: ffc565f4-5cb2-4d0d-bc8f-395880e43eec
Public Version Date: August 15, 2025
Public Version Number: 7
DI Record Publish Date: October 05, 2015