FDA UDI In Commercial Distribution 🇺🇸 United States

RegenerOss

DI: 00813954025322 · Model: RGP1020 · COLLAGEN MATRIX, INC.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
RegenerOss
Primary DI
00813954025322
Version / Model
RGP1020
Company Name
COLLAGEN MATRIX, INC.
Labeler DUNS
176262442
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-01-06
Public Version
1
Public Version Date
2023-01-16
Public Version Status
New
Public Device Record Key
6888be40-5eda-4532-8814-dca7b5374dbb

Device Description

Bone Graft Plug

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
NPM Bone Grafting Material, Animal Source
LYC Bone Grafting Material, Synthetic

GMDN Terms

Code Name
47971 Dental bone matrix implant, synthetic

Identifiers

Type ID
Package 10813954025329
Primary 00813954025322

Customer Contacts

Phone
15617766700

Device Sizes

Type Value Unit Text
Device Size Text, specify Diameter: 10mm
Device Size Text, specify Length: 20mm

Storage Conditions

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