FDA UDI In Commercial Distribution 🇺🇸 United States

GLOBAL AP

DI: 10603295090670 · Model: 2130-02-000 · DEPUY ORTHOPAEDICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
GLOBAL AP
Primary DI
10603295090670
Version / Model
2130-02-000
Catalog Number
213002000
Company Name
DEPUY ORTHOPAEDICS, INC.
Labeler DUNS
080506581
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
07d2f742-f9ab-4458-ac2b-e807dbd77d81

Device Description

GLOBAL AP REVISION TRIAL INSERT

Device Characteristics

Single Use
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HWT TEMPLATE

GMDN Terms

Code Name
58804 Surgical implant template, single-use

Identifiers

Type ID
Primary 10603295090670

Customer Contacts