FDA UDI In Commercial Distribution 🇺🇸 United States

Kerrison Ronguer

DI: 00192896116221 · Model: 404-342C · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Kerrison Ronguer
Primary DI
00192896116221
Version / Model
404-342C
Catalog Number
404-342C
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-12-20
Public Version
1
Public Version Date
2023-12-28
Public Version Status
New
Public Device Record Key
b977208e-0fec-4829-b362-5d597a6872a1

Device Description

Convertible Kerrison Ronguer With Ejector Pin 10 Millimeter Opening 40° Up-Angle 6 Millimeter Bite

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
["Dry Heat Sterilization", "Moist Heat or Steam Sterilization"]

Product Codes

Code Name
HTX RONGEUR

GMDN Terms

Code Name
32853 Orthopaedic joint/limb rongeur

Identifiers

Type ID
Primary 00192896116221

Customer Contacts

Device Sizes

Type Value Unit Text
Length 8 Inch