FDA UDI In Commercial Distribution 🇺🇸 United States

Matira

DI: B073K0730000 · Model: 07-K07-3000 · Kalitec Direct LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Matira
Primary DI
B073K0730000
Version / Model
07-K07-3000
Catalog Number
07-K07-3000
Company Name
Kalitec Direct LLC
Labeler DUNS
041956211
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-01-03
Public Version
1
Public Version Date
2020-01-13
Public Version Status
New
Public Device Record Key
a8ea7e76-ec04-4b20-abf5-4eb42230fff2

Device Description

Plate Bender, Universal

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
No
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
HXW Bender

GMDN Terms

Code Name
44795 Manual orthopaedic bender, reusable

Identifiers

Type ID
Primary B073K0730000