FDA UDI In Commercial Distribution 🇺🇸 United States

PATHWAY

DI: 10603295226451 · Model: 9505-01-508 · DEPUY INTERNATIONAL LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PATHWAY
Primary DI
10603295226451
Version / Model
9505-01-508
Catalog Number
950501508
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
1
Public Version Date
2018-10-25
Public Version Status
New
Public Device Record Key
cbf3291d-6bfb-4aa4-bcd4-784ce025b5eb

Device Description

M.B.T. PATHWAY TIBIAL TEMPLATE SIZE 5

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
HWT TEMPLATE

GMDN Terms

Code Name
46479 Surgical implant template, reusable

Identifiers

Type ID
Primary 10603295226451

Customer Contacts