FDA UDI In Commercial Distribution 🇺🇸 United States

OsseoFit™ Subscapularis Kit (Bone Tunnel)

DI: 00840277405005 · Model: 120002051 · RIVERPOINT MEDICAL, LLC
Product Codes
0
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
OsseoFit™ Subscapularis Kit (Bone Tunnel)
Primary DI
00840277405005
Version / Model
120002051
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
d4f27782-264e-4de3-be28-0d3d64a5f6c4

Device Description

Subscapularis Repair Suture Kit-Bone Tunnel

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 00840277405005