FDA UDI In Commercial Distribution 🇺🇸 United States

Sontec Kerrison Rongeur

DI: 00192896117594 · Model: 404-540EJ · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Sontec Kerrison Rongeur
Primary DI
00192896117594
Version / Model
404-540EJ
Catalog Number
404-540EJ
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-05-13
Public Version
1
Public Version Date
2024-05-21
Public Version Status
New
Public Device Record Key
9cc27a47-c3d8-4b82-a147-ad82e493d013

Device Description

Sontec Kerrison Rongeur Without Eject Pin 40° Forward Up-Angled 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

Product Codes

Code Name
HTX RONGEUR

GMDN Terms

Code Name
32853 Orthopaedic joint/limb rongeur

Identifiers

Type ID
Primary 00192896117594

Customer Contacts

Device Sizes

Type Value Unit Text
Length 7 Inch
Device Size Text, specify Bite Width 2 Millimeter