FDA UDI Not in Commercial Distribution 🇺🇸 United States

NEOFIT

DI: 03760225713198 · Model: P01 30011 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
NEOFIT
Primary DI
03760225713198
Version / Model
P01 30011
Catalog Number
P01 30011
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-13
Public Version
3
Public Version Date
2025-05-07
Public Version Status
Update
Public Device Record Key
c4e22def-2c08-4758-ab91-3e9807da3084
Distribution End Date
2025-05-06

Device Description

NEOFIT BURRS KIT

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
FSM TRAY, SURGICAL, INSTRUMENT

GMDN Terms

Code Name
12143 Instrument tray, reusable

Identifiers

Type ID
Primary 03760225713198

Customer Contacts