FDA UDI In Commercial Distribution 🇺🇸 United States

OsseoFit™ Subscapularis Kit (Suture Anchor)

DI: 00840277404992 · Model: 120002050 · RIVERPOINT MEDICAL, LLC
Product Codes
0
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OsseoFit™ Subscapularis Kit (Suture Anchor)
Primary DI
00840277404992
Version / Model
120002050
Company Name
RIVERPOINT MEDICAL, LLC
Labeler DUNS
964053560
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-31
Public Version
1
Public Version Date
2025-01-08
Public Version Status
New
Public Device Record Key
7bdf816f-8e5f-4c81-8d2b-6cc82d76ff08

Device Description

Subscapularis Repair Suture Kit-Suture Anchor

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
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
Yes
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

GMDN Terms

Code Name
13907 Polyolefin/fluoropolymer suture, multifilament
13909 Polyolefin/fluoropolymer suture, monofilament

Identifiers

Type ID
Primary 00840277404992