FDA UDI In Commercial Distribution 🇺🇸 United States

RIVERLON

DI: 00810020084689 · Model: 669BK · RIVERPOINT MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
RIVERLON
Primary DI
00810020084689
Version / Model
669BK
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
2
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
3c2e5b2e-f9a6-41dc-a40e-1519c6033195

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
GAR Suture, Nonabsorbable, Synthetic, Polyamide

GMDN Terms

Code Name
38000 Nylon suture, non-bioabsorbable, monofilament

Identifiers

Type ID
Package 10810020084686
Primary 00810020084689