FDA UDI In Commercial Distribution 🇺🇸 United States

BAYONET CURETTE

DI: 00192896036758 · Model: 413-040 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BAYONET CURETTE
Primary DI
00192896036758
Version / Model
413-040
Catalog Number
413-040
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-13
Public Version
2
Public Version Date
2019-09-10
Public Version Status
Update
Public Device Record Key
fae9c6f9-3c31-4389-aa9b-8c7c66a9388d

Device Description

BAYONET CURETTE BENDING HYPOPHYSIS ENUCLEATOR 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
["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 00192896036758

Customer Contacts

Device Sizes

Type Value Unit Text
Length 8.75 Inch