FDA UDI In Commercial Distribution 🇺🇸 United States

RPF PATHWAY

DI: 10603295226833 · Model: 9505-01-550 · DEPUY INTERNATIONAL LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RPF PATHWAY
Primary DI
10603295226833
Version / Model
9505-01-550
Catalog Number
950501550
Company Name
DEPUY INTERNATIONAL LTD
Labeler DUNS
896498813
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-24
Public Version
3
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
86fb96d0-e793-4317-96f3-ae8f76ec3ab5

Device Description

RPF PATHWAY FEMORAL 3 IN 1 SIZE 1

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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 10603295226833

Customer Contacts