FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867413498 · Model: AR-3200-0021R · ARTHREX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Arthrex®
Primary DI
00888867413498
Version / Model
AR-3200-0021R
Catalog Number
AR-3200-0021R
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-07-07
Public Version
1
Public Version Date
2022-07-15
Public Version Status
New
Public Device Record Key
d9b51914-373d-4bd6-868b-30e09098c562

Device Description

CCU, ARTHREX SYNERGY UHD4,REFURB

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
GCJ Laparoscope, general & plastic surgery

GMDN Terms

Code Name
35958 Endoscope video camera

Identifiers

Type ID
Primary 00888867413498

Customer Contacts