FDA UDI In Commercial Distribution 🇺🇸 United States

RIVERPRO

DI: 00810020084788 · Model: P8776 · RIVERPOINT MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
RIVERPRO
Primary DI
00810020084788
Version / Model
P8776
Company Name
RIVERPOINT MEDICAL, LLC
Labeler DUNS
964053560
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-18
Public Version
3
Public Version Date
2023-06-02
Public Version Status
Update
Public Device Record Key
81c4993d-5de1-45b7-b7d3-b07d518254f7

Device Description

Suture

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GAW Suture, Nonabsorbable, Synthetic, Polypropylene

GMDN Terms

Code Name
13909 Polyolefin/fluoropolymer suture, monofilament

Identifiers

Type ID
Package 10810020084785
Primary 00810020084788