FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867088399 · Model: AR-13200PA-20.0R · ARTHREX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Arthrex®
Primary DI
00888867088399
Version / Model
AR-13200PA-20.0R
Catalog Number
AR-13200PA-20.0R
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-15
Public Version
20
Public Version Date
2023-11-23
Public Version Status
Update
Public Device Record Key
20769c9f-6129-40a8-a7c7-e4665920f85d

Device Description

20MM RT,TIB A/P SLPD OSTEO PLT

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
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
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
HRS PLATE, FIXATION, BONE

GMDN Terms

Code Name
46647 Orthopaedic fixation plate, non-bioabsorbable

Identifiers

Type ID
Primary 00888867088399
Secondary M150AR13200PA200R0

Customer Contacts