FDA UDI In Commercial Distribution 🇺🇸 United States

Life Instruments

DI: M930830120200 · Model: 830-1202-0 · Life Instrument Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Life Instruments
Primary DI
M930830120200
Version / Model
830-1202-0
Company Name
Life Instrument Corporation
Labeler DUNS
948025002
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-02-26
Public Version
1
Public Version Date
2021-03-08
Public Version Status
New
Public Device Record Key
c1c5e49b-749c-4f44-ab24-216ae288ad2a

Device Description

12" Anterior Kerrison 2mm 40° Fwd

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
No
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
HTX Rongeur

GMDN Terms

Code Name
32853 Orthopaedic joint/limb rongeur

Identifiers

Type ID
Primary M930830120200