FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867267220 · Model: AR-9821 · ARTHREX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Arthrex®
Primary DI
00888867267220
Version / Model
AR-9821
Catalog Number
AR-9821
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-03-13
Public Version
24
Public Version Date
2024-02-08
Public Version Status
Update
Public Device Record Key
279aa424-2b9e-4799-ab92-beba945d2484

Device Description

ApolloRF™ XL90, Aspirating Ablator 90°

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
Secondary M150AR98211
Primary 00888867267220

Customer Contacts