FDA UDI In Commercial Distribution 🇺🇸 United States

ACTIS

DI: 10603295548652 · Model: 3010-01-060 · DEPUY (IRELAND)
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ACTIS
Primary DI
10603295548652
Version / Model
3010-01-060
Catalog Number
301001060
Company Name
DEPUY (IRELAND)
Labeler DUNS
989365556
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-04-01
Public Version
1
Public Version Date
2022-04-11
Public Version Status
New
Public Device Record Key
5b2f69fd-5242-419e-ae49-729408dd68c6

Device Description

ACTIS HIP SYSTEM BROACH SIZE 6

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
QBO Instruments designed for press-fit osteochondral implants

GMDN Terms

Code Name
36167 Orthopaedic broach

Identifiers

Type ID
Primary 10603295548652

Customer Contacts