FDA UDI In Commercial Distribution 🇺🇸 United States

DEPUY SYNTHES

DI: 10603295509295 · Model: 483036120 · DEPUY (IRELAND)
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DEPUY SYNTHES
Primary DI
10603295509295
Version / Model
483036120
Catalog Number
483036120
Company Name
DEPUY (IRELAND)
Labeler DUNS
989365556
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-04-01
Public Version
1
Public Version Date
2024-04-09
Public Version Status
New
Public Device Record Key
889465c0-493f-40b6-bd18-8bcbf39103ab

Device Description

DEPUY SYNTHES 36 MM +12 TRIAL HEAD

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
HWT TEMPLATE

GMDN Terms

Code Name
58479 Femoral head prosthesis trial

Identifiers

Type ID
Primary 10603295509295

Customer Contacts