FDA UDI In Commercial Distribution 🇺🇸 United States

Sontec Kerrison Rongeur

DI: 00192896106901 · Model: 404-5391 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Sontec Kerrison Rongeur
Primary DI
00192896106901
Version / Model
404-5391
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-02-25
Public Version
1
Public Version Date
2021-03-05
Public Version Status
New
Public Device Record Key
5f6da3fc-8978-4f81-82ed-5a92eb313fc3

Device Description

Sontec Kerrison Rongeur 40 Degree Forward 1.5 Millimeters

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 00192896106901

Customer Contacts

Device Sizes

Type Value Unit Text
Length 7 Inch