FDA UDI In Commercial Distribution 🇺🇸 United States

ACTIS

DI: 10603295393641 · Model: 2010-01-020 · DEPUY (IRELAND)
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ACTIS
Primary DI
10603295393641
Version / Model
2010-01-020
Catalog Number
201001020
Company Name
DEPUY (IRELAND)
Labeler DUNS
989365556
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-11-13
Public Version
4
Public Version Date
2019-08-02
Public Version Status
Update
Public Device Record Key
3b9d2e3b-34b2-4db6-90d3-5a9be7e055f7

Device Description

ACTIS BROACH SIZE 2

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
Yes
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
HTQ BROACH

GMDN Terms

Code Name
36167 Orthopaedic broach

Identifiers

Type ID
Primary 10603295393641

Customer Contacts