FDA UDI In Commercial Distribution 🇺🇸 United States

SONTEC KERRISON RONGEUR

DI: 00192896096646 · Model: 404-539Q · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SONTEC KERRISON RONGEUR
Primary DI
00192896096646
Version / Model
404-539Q
Catalog Number
404-539Q
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-05-03
Public Version
3
Public Version Date
2021-03-23
Public Version Status
Update
Public Device Record Key
d88680e7-16e5-4ff9-a9ed-4ab6cb4c16b2

Device Description

SONTEC KERRISON RONGEUR FORWARD TIP QUANTUM

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

Product Codes

Code Name
HTX Rongeur

GMDN Terms

Code Name
32853 Orthopaedic joint/limb rongeur

Identifiers

Type ID
Primary 00192896096646

Customer Contacts

Phone
800-821-7496

Device Sizes

Type Value Unit Text
Length 7 Inch
Device Size Text, specify 1 Millimeter Tip