FDA UDI In Commercial Distribution 🇺🇸 United States

NEUROSURGICAL CURETTE

DI: 00192896036765 · Model: 413-045 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
NEUROSURGICAL CURETTE
Primary DI
00192896036765
Version / Model
413-045
Catalog Number
413-045
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-12
Public Version
2
Public Version Date
2025-09-19
Public Version Status
Update
Public Device Record Key
2d2b3493-4979-4d4c-aa4b-fb7f01b8fce0

Device Description

NEUROSURGICAL CURETTE KNURLED HANDLE STRAIGHT RING TIP TITANIUM

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
Yes
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
Dry Heat Sterilization, Moist Heat or Steam Sterilization

Product Codes

Code Name
HTF Curette

GMDN Terms

Code Name
66306 Neurosurgical curette, reusable

Identifiers

Type ID
Primary 00192896036765

Customer Contacts

Device Sizes

Type Value Unit Text
Length 8.25 Inch
Device Size Text, specify 3 Millimeter Tip