FDA UDI In Commercial Distribution 🇺🇸 United States

Life Instruments

DI: M93071018002C0 · Model: 710-1800-2C · Life Instrument Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Life Instruments
Primary DI
M93071018002C0
Version / Model
710-1800-2C
Company Name
Life Instrument Corporation
Labeler DUNS
948025002
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-14
Public Version
1
Public Version Date
2020-12-22
Public Version Status
New
Public Device Record Key
0d5a8fb0-81a6-4769-acec-57f0cd3daa08

Device Description

18" Anterior Curette Reverse-Angled 9" Handle

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
FZS Curette, Surgical, General Use

GMDN Terms

Code Name
31335 Bone curette, reusable

Identifiers

Type ID
Primary M93071018002C0