FDA UDI Not in Commercial Distribution 🇺🇸 United States

NEUFLEX

DI: 10603295149484 · Model: 2633-22-000 · DEPUY ORTHOPAEDICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NEUFLEX
Primary DI
10603295149484
Version / Model
2633-22-000
Catalog Number
263322000
Company Name
DEPUY ORTHOPAEDICS, INC.
Labeler DUNS
080506581
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-24
Public Version
3
Public Version Date
2022-03-31
Public Version Status
Update
Public Device Record Key
d18e1055-70b5-4b11-90d4-149e956e0fe8
Distribution End Date
2022-03-31

Device Description

NEUFLEX PIP BROACH DISTAL SIZE 2

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
HTQ BROACH

GMDN Terms

Code Name
36167 Orthopaedic broach

Identifiers

Type ID
Primary 10603295149484

Customer Contacts