FDA UDI In Commercial Distribution 🇺🇸 United States

MiroDerm Fenestrated

DI: 00857072005163 · Model: BLM-200-02-0303 · REPRISE BIOMEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MiroDerm Fenestrated
Primary DI
00857072005163
Version / Model
BLM-200-02-0303
Company Name
REPRISE BIOMEDICAL, INC.
Labeler DUNS
043611421
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-30
Public Version
1
Public Version Date
2020-10-08
Public Version Status
New
Public Device Record Key
73263ed1-ccb3-4904-ae4c-a1c66090506d

Device Description

3 x 3 cm Fenestrated Biologic Wound 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
MR Safe
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
KGN Dressing, Wound, Collagen

GMDN Terms

Code Name
45023 Collagen wound matrix dressing

Identifiers

Type ID
Primary 00857072005163

Customer Contacts

Phone
952-377-8238

Premarket Submissions

Submission Number Supplement Number
K143426 000