FDA UDI In Commercial Distribution 🇺🇸 United States

Tenodesis Screw System

DI: 00889795057570 · Model: P41-900-BASE · PARAGON 28, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Tenodesis Screw System
Primary DI
00889795057570
Version / Model
P41-900-BASE
Catalog Number
P41-900-BASE
Company Name
PARAGON 28, INC.
Labeler DUNS
042961576
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-10-17
Public Version
3
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
381d6ac5-52dd-403b-948a-d78b1495bcb7

Device Description

Grappler Interference Screw Instruments, Caddy

Device Characteristics

Single Use
No
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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
FSM TRAY, SURGICAL, INSTRUMENT

GMDN Terms

Code Name
13730 Device sterilization/disinfection container, reusable

Identifiers

Type ID
Primary 00889795057570