FDA UDI In Commercial Distribution 🇺🇸 United States

FERRIS SMITH RONGEUR

DI: 00192896095564 · Model: 404-822 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FERRIS SMITH RONGEUR
Primary DI
00192896095564
Version / Model
404-822
Catalog Number
404-822
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-25
Public Version
2
Public Version Date
2019-07-12
Public Version Status
Update
Public Device Record Key
bbec907f-aaee-47a6-b4b4-1d69b3483528

Device Description

FERRIS SMITH RONGEUR STRAIGHT SERRATED TIP

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 00192896095564

Customer Contacts

Phone
800-821-7496

Device Sizes

Type Value Unit Text
Length 12 Inch
Device Size Text, specify 4 x 10 Millimeter Tip