FDA UDI In Commercial Distribution 🇺🇸 United States

FERRIS SMITH ARTHROSCOPIC RONGEUR

DI: 00192896035263 · Model: 404-802LP · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FERRIS SMITH ARTHROSCOPIC RONGEUR
Primary DI
00192896035263
Version / Model
404-802LP
Catalog Number
404-802LP
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-11
Public Version
2
Public Version Date
2019-07-12
Public Version Status
Update
Public Device Record Key
f02aa390-8f8c-4244-ac21-912b66389cb8

Device Description

FERRIS SMITH ARTHROSCOPIC RONGEUR UP-ANGLE SHAFT LOW PROFILE

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
["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 00192896035263

Customer Contacts

Device Sizes

Type Value Unit Text
Length 7 Inch
Device Size Text, specify 4 x 10 Millimeter Tip