FDA UDI In Commercial Distribution 🇺🇸 United States

HemiCAP®

DI: M528800712050 · Model: 8007-1205 · ARTHROSURFACE INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HemiCAP®
Primary DI
M528800712050
Version / Model
8007-1205
Catalog Number
8007-1205
Company Name
ARTHROSURFACE INCORPORATED
Labeler DUNS
144666109
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-20
Public Version
3
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
3450d542-6e79-408e-8e3a-74122bb5eef4

Device Description

Kit, 2.5mm Guide Pin (5 Pk)

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
35685 Orthopaedic bone wire

Identifiers

Type ID
Primary M528800712050

Customer Contacts

Phone
508-520-3003