FDA UDI In Commercial Distribution 🇺🇸 United States

GLOBAL AP

DI: 10603295090656 · Model: 2130-01-120 · DEPUY ORTHOPAEDICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
GLOBAL AP
Primary DI
10603295090656
Version / Model
2130-01-120
Catalog Number
213001120
Company Name
DEPUY ORTHOPAEDICS, INC.
Labeler DUNS
080506581
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-06-15
Public Version
1
Public Version Date
2018-07-16
Public Version Status
New
Public Device Record Key
804ceac7-7e7d-4fd1-9659-f2e7de69e11c

Device Description

GLOBAL AP HUMERAL HEAD DISTRACTOR

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
HWB EXTRACTOR

GMDN Terms

Code Name
47866 Orthopaedic implant/instrument dismantling device

Identifiers

Type ID
Primary 10603295090656

Customer Contacts