FDA UDI In Commercial Distribution 🇺🇸 United States

CarpalFiX

DI: M78012730222 · Model: 127-30222 · EXTREMITY MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CarpalFiX
Primary DI
M78012730222
Version / Model
127-30222
Company Name
EXTREMITY MEDICAL, LLC
Labeler DUNS
832720358
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-14
Public Version
4
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
a1529ba6-b301-4558-9684-fa59433fa3cd

Device Description

Lag Screw (Cannulated Tapered) 3.0 x 22mm

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
No
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
HWC Screw, Fixation, Bone

GMDN Terms

Code Name
56642 Orthopaedic bone screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary M78012730222

Premarket Submissions

Submission Number Supplement Number
K121349 000