FDA UDI In Commercial Distribution 🇺🇸 United States

ProgenaMatrix

DI: 00850017159013 · Model: PM3003 · Progenacare Global, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ProgenaMatrix
Primary DI
00850017159013
Version / Model
PM3003
Company Name
Progenacare Global, LLC
Labeler DUNS
054791028
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-04-06
Public Version
1
Public Version Date
2023-04-14
Public Version Status
New
Public Device Record Key
b1824959-0865-4a97-83bc-4127d1f1f1be

Device Description

Human Keratin 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 Wound Dressing With Animal-Derived Material(S)

GMDN Terms

Code Name
45023 Collagen wound matrix dressing

Identifiers

Type ID
Primary 00850017159013

Customer Contacts

Phone
770-627-2547

Premarket Submissions

Submission Number Supplement Number
K182010 000

Device Sizes

Type Value Unit Text
Length 3 Centimeter
Width 3 Centimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 30 Degrees Celsius