FDA UDI In Commercial Distribution 🇺🇸 United States

MicroMatrix®

DI: 00386190002056 · Model: MMFX05 · ACELL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MicroMatrix®
Primary DI
00386190002056
Version / Model
MMFX05
Catalog Number
MMFX05
Company Name
ACELL, INC.
Labeler DUNS
137258252
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-02
Public Version
1
Public Version Date
2023-10-10
Public Version Status
New
Public Device Record Key
b97ff30c-3e68-45bf-a238-5b15de2ddd4a

Device Description

MicroMatrix® Flex 5cc

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 Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
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 Wound dressing with animal-derived material(s)

GMDN Terms

Code Name
45023 Collagen wound matrix dressing

Identifiers

Type ID
Primary 00386190002056

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K230980 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 5cc Total Volume

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a clean, dry environment at room temperature