FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867320253 · Model: AR-9835 · ARTHREX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Arthrex®
Primary DI
00888867320253
Version / Model
AR-9835
Catalog Number
AR-9835
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-11-26
Public Version
3
Public Version Date
2019-07-23
Public Version Status
Update
Public Device Record Key
e3646d5c-9714-4f63-8dbb-4806a5286216

Device Description

Apollo RF® H50, Aspirating, Ablator, 50°

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, cutting & coagulation & accessories

GMDN Terms

Code Name
61872 Endoscopic electrosurgical electrode, bipolar, single-use

Identifiers

Type ID
Primary 00888867320253

Customer Contacts