FDA UDI In Commercial Distribution 🇺🇸 United States

Bayonet Curette

DI: 00192896104853 · Model: 413-052 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Bayonet Curette
Primary DI
00192896104853
Version / Model
413-052
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-21
Public Version
1
Public Version Date
2020-09-29
Public Version Status
New
Public Device Record Key
4c2dd9ee-bfd4-4f14-83ba-ebe00db5e6fc

Device Description

Bayonet Curette Knurl Handle 45 Degrees Up Angle 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
Yes
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
["Moist Heat or Steam Sterilization", "Dry Heat Sterilization"]

Product Codes

Code Name
HTF CURETTE

GMDN Terms

Code Name
62558 General-purpose curette

Identifiers

Type ID
Primary 00192896104853

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Tip 2.25 Millimeter
Length 10.25 Inch