FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867458024 · Model: ABS-4062 · ARTHREX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Arthrex®
Primary DI
00888867458024
Version / Model
ABS-4062
Catalog Number
ABS-4062
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-05-29
Public Version
2
Public Version Date
2025-12-08
Public Version Status
Update
Public Device Record Key
8a8449bd-3699-40cf-b1fa-74b16c69eaab

Device Description

JumpStart ClearFit 6.0" x 6.0"

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 Unsafe
Direct Marking Exempt
No
PM Exempt
No
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
FRO Dressing, wound, drug

GMDN Terms

Code Name
62983 Bioelectric wound dressing

Identifiers

Type ID
Primary 00888867458024

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K180533 000