FDA UDI In Commercial Distribution 🇺🇸 United States

Tenodesis Screw System

DI: 00889795057396 · Model: P41-920-0001 · PARAGON 28, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Tenodesis Screw System
Primary DI
00889795057396
Version / Model
P41-920-0001
Catalog Number
P41-920-0001
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
1
Public Version Date
2019-10-25
Public Version Status
New
Public Device Record Key
6cecf9cc-5c47-4e51-b3b4-79ecdb8c970e

Device Description

Tendon Sizer, Grappler

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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
46479 Surgical implant template, reusable

Identifiers

Type ID
Primary 00889795057396