FDA UDI In Commercial Distribution 🇺🇸 United States

Meso BioMatrix® Acellular Peritoneum Matrix

DI: 00812337025300 · Model: 30063-01 · DSM BIOMEDICAL, INC.
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Meso BioMatrix® Acellular Peritoneum Matrix
Primary DI
00812337025300
Version / Model
30063-01
Catalog Number
910204
Company Name
DSM BIOMEDICAL, INC.
Labeler DUNS
131107757
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-08
Public Version
6
Public Version Date
2023-10-04
Public Version Status
Update
Public Device Record Key
eac76281-a261-4c5a-be7a-2b7e7e86fc36

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FTM Mesh, Surgical
OXE Mesh, Surgical, Collagen, Staple Line Reinforcement
OXH Mesh, Surgical, Collagen, Plastic And Reconstructive Surgery
PAG Mesh, Surgical, Non-Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or Transobturator
PAJ Mesh, Surgical, Non-Synthetic, Urogynecologic, For Apical Vaginal And Uterine Prolapse, Transabdominally Placed

GMDN Terms

Code Name
60907 Extra-gynaecological surgical mesh, collagen, bioabsorbable, non-antimicrobial

Identifiers

Type ID
Primary 00812337025300

Customer Contacts

Phone
484-713-2100

Device Sizes

Type Value Unit Text
Width 2 Centimeter
Length 4 Centimeter