FDA UDI Not in Commercial Distribution 🇺🇸 United States

MIROMESH®

DI: 00857072005033 · Model: BLM-100-01-0816 · REPRISE BIOMEDICAL, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MIROMESH®
Primary DI
00857072005033
Version / Model
BLM-100-01-0816
Company Name
REPRISE BIOMEDICAL, INC.
Labeler DUNS
043611421
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-09
Public Version
8
Public Version Date
2023-10-04
Public Version Status
Update
Public Device Record Key
569ed090-dc5a-4a4c-bd27-11c892508737
Distribution End Date
2023-07-31

Device Description

Biologic Matrix

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
OXH Mesh, Surgical, Collagen, Plastic And Reconstructive Surgery

GMDN Terms

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

Identifiers

Type ID
Primary 00857072005033

Customer Contacts

Phone
952-377-8238

Device Sizes

Type Value Unit Text
Width 8 Centimeter
Height 16 Centimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 30 Degrees Celsius