FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex

DI: B504AR87030 · Model: AR-8703 · Provision
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Arthrex
Primary DI
B504AR87030
Version / Model
AR-8703
Company Name
Provision
Labeler DUNS
016889401
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-20
Public Version
3
Public Version Date
2020-12-04
Public Version Status
Update
Public Device Record Key
ab4a6384-b8b7-4cfe-a6b8-08a87c17ad7c

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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HWQ Passer

GMDN Terms

Code Name
61823 Suturing unit, reprocessed

Identifiers

Type ID
Package B504AR87031
Primary B504AR87030

Customer Contacts

Phone
541-480-7953