FDA UDI In Commercial Distribution 🇺🇸 United States

Profiniti

DI: 00813954025339 · Model: AFP02 · COLLAGEN MATRIX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Profiniti
Primary DI
00813954025339
Version / Model
AFP02
Catalog Number
AFP02
Company Name
COLLAGEN MATRIX, INC.
Labeler DUNS
176262442
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-02-20
Public Version
1
Public Version Date
2023-02-28
Public Version Status
New
Public Device Record Key
4a0b67dd-5d5d-4dfb-b5e0-6a582dc1693e

Device Description

Moldable Putty Bone Graft 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
MQV Filler, Bone Void, Calcium Compound

GMDN Terms

Code Name
46425 Bone matrix implant, animal-derived, bioabsorbable

Identifiers

Type ID
Primary 00813954025339

Device Sizes

Type Value Unit Text
Device Size Text, specify 2cc

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
59 – 86 Degrees Fahrenheit