FDA UDI In Commercial Distribution 🇺🇸 United States

HemiCAP®

DI: M5289P0710020 · Model: 9P07-1002 · ARTHROSURFACE INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HemiCAP®
Primary DI
M5289P0710020
Version / Model
9P07-1002
Catalog Number
9P07-1002
Company Name
ARTHROSURFACE INCORPORATED
Labeler DUNS
144666109
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-14
Public Version
3
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
c94a6a94-e5ad-4c04-b8fa-929981b4aff9

Device Description

1.5mm Pin Kit, ToeMOTION

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
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
LZJ Prosthesis, Toe (Metatarsophalangeal), Joint, Metal/Polymer, Semi-Constrained

GMDN Terms

Code Name
35685 Orthopaedic bone wire

Identifiers

Type ID
Primary M5289P0710020

Customer Contacts

Phone
508-520-3003

Device Sizes

Type Value Unit Text
Outer Diameter 1.5 Millimeter