FDA UDI In Commercial Distribution 🇺🇸 United States

KERRISON RONGEUR

DI: 00192896033542 · Model: 404-407 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KERRISON RONGEUR
Primary DI
00192896033542
Version / Model
404-407
Catalog Number
404-407
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-10
Public Version
2
Public Version Date
2019-07-12
Public Version Status
Update
Public Device Record Key
b19c1580-295d-477a-baf8-5c3aa7873b4e

Device Description

KERRISON BAYONET RONGEUR WITHOUT EJECTION PIN ANGLED TIP THIN FOOTPLATE

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
No
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 00192896033542

Customer Contacts

Device Sizes

Type Value Unit Text
Length 8 Inch
Device Size Text, specify 4 Millimeter Tip
Device Size Text, specify 40 Degree Tip