FDA UDI In Commercial Distribution 🇺🇸 United States

KERRISON RONGEUR

DI: 00192896094642 · Model: 404-6075 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KERRISON RONGEUR
Primary DI
00192896094642
Version / Model
404-6075
Catalog Number
404-6075
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-07
Public Version
3
Public Version Date
2023-04-11
Public Version Status
Update
Public Device Record Key
102f764b-36ef-4118-bfda-e1d06b1bc3d5

Device Description

KERRISON UNIVERSAL ROTATING RONGEUR WITH SHAFT LOCK AND TISSUE EJECTOR PIN

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
No
Has Manufacturing Date
No
Has Expiration Date
Yes
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 00192896094642

Customer Contacts

Device Sizes

Type Value Unit Text
Length 8 Inch
Device Size Text, specify 90 Degree Tip
Device Size Text, specify 5 Millimeter Bite