FDA UDI In Commercial Distribution 🇺🇸 United States

n/a

DI: 05060267130785 · Model: 202-1137 · XIROS LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
n/a
Primary DI
05060267130785
Version / Model
202-1137
Catalog Number
n/a
Company Name
XIROS LTD
Labeler DUNS
228209805
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-16
Public Version
6
Public Version Date
2023-07-28
Public Version Status
Update
Public Device Record Key
ab0163a2-07ed-4650-b9a6-0c7f3ab3e845

Device Description

Impactor Assembly

Device Characteristics

Single Use
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
HXJ Staple Driver

GMDN Terms

Code Name
12696 Orthopaedic implant inserter/extractor, reusable

Identifiers

Type ID
Primary 05060267130785

Customer Contacts