FDA UDI In Commercial Distribution 🇺🇸 United States

ACTIS

DI: 10603295380641 · Model: 1010-13-005 · DEPUY (IRELAND)
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ACTIS
Primary DI
10603295380641
Version / Model
1010-13-005
Catalog Number
101013005
Company Name
DEPUY (IRELAND)
Labeler DUNS
989365556
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-02-22
Public Version
3
Public Version Date
2023-06-26
Public Version Status
Update
Public Device Record Key
d9a770ef-59b2-4579-9f25-b873f6a90e65

Device Description

ACTIS DUOFIX HIP PROSTHESIS FEMORAL STEM 12/14 TAPER CEMENTLESS STD COLLAR SIZE 0 Non-CE

Device Characteristics

Single Use
Yes
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
No
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
KWL Prosthesis, hip, hemi-, femoral, metal
KWY Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented
LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED
MEH Prosthesis, hip, semi-constrained, uncemented, metal / polymer, non-porous, calcium phosphate

GMDN Terms

Code Name
64708 Coated femoral stem prosthesis, one-piece

Identifiers

Type ID
Primary 10603295380641

Customer Contacts