FDA UDI In Commercial Distribution 🇺🇸 United States

KLOSURE

DI: 00812444027020 · Model: 9626013381 · RIVERPOINT MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
KLOSURE
Primary DI
00812444027020
Version / Model
9626013381
Company Name
RIVERPOINT MEDICAL, LLC
Labeler DUNS
964053560
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-11-06
Public Version
7
Public Version Date
2023-06-02
Public Version Status
Update
Public Device Record Key
0e54749e-c32d-4b5b-887e-270427075c3b

Device Description

Suture

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
GAW Suture, Nonabsorbable, Synthetic, Polypropylene

GMDN Terms

Code Name
13909 Polyolefin/fluoropolymer suture, monofilament

Identifiers

Type ID
Package 10812444027027
Primary 00812444027020