FDA UDI In Commercial Distribution 🇺🇸 United States

RIGIDFIX

DI: 10886705020102 · Model: 213029 · DEPUY MITEK, LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RIGIDFIX
Primary DI
10886705020102
Version / Model
213029
Catalog Number
213029
Company Name
DEPUY MITEK, LLC
Labeler DUNS
190572854
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-01
Public Version
4
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
174a6d4b-4929-4a92-96ea-bf9b7d99c3e7

Device Description

RIGIDFIX CURVE Femoral Rod Soft Tissue Only 8mm, 30-110mm (Plus or Minus 6 Percent)

Device Characteristics

Single Use
No
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
No
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
MAI FASTENER, FIXATION, BIODEGRADABLE, SOFT TISSUE
HTY PIN, FIXATION, SMOOTH

GMDN Terms

Code Name
46165 Orthopaedic guidewire, reusable

Identifiers

Type ID
Primary 10886705020102

Customer Contacts