FDA UDI In Commercial Distribution 🇺🇸 United States

Life Instruments

DI: M93051414031RT20 · Model: 514-1403-1RT-2 · Life Instrument Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Life Instruments
Primary DI
M93051414031RT20
Version / Model
514-1403-1RT-2
Company Name
Life Instrument Corporation
Labeler DUNS
948025002
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-11-05
Public Version
1
Public Version Date
2021-11-15
Public Version Status
New
Public Device Record Key
307ab57e-90de-4f41-8c74-1aa4b7d2f27b

Device Description

#3 Toothed Curette Bayonet Angled Up, Right Facing

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 M93051414031RT20