FDA UDI In Commercial Distribution 🇺🇸 United States

Cushing Intervertebral Disc Rongeur

DI: 00192896106536 · Model: 404-724 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Cushing Intervertebral Disc Rongeur
Primary DI
00192896106536
Version / Model
404-724
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-01-26
Public Version
1
Public Version Date
2021-02-03
Public Version Status
New
Public Device Record Key
753e6b8d-cefc-4bad-8181-cf416cec89b2

Device Description

Cushing Intervertebral Disc Rongeur 2 X 10 Millimeter Straight

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 00192896106536

Customer Contacts

Device Sizes

Type Value Unit Text
Length 9 Inch