FDA UDI In Commercial Distribution 🇺🇸 United States

CARTILAGE CRUSHER

DI: 00192896032057 · Model: 350-850 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CARTILAGE CRUSHER
Primary DI
00192896032057
Version / Model
350-850
Catalog Number
350-850
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-17
Public Version
3
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
f5d2a103-5d20-47ff-afed-f363d282ceae

Device Description

CARTILAGE CRUSHER HAND CONTROLLED CRANK SERRATED BED

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
HWN INSTRUMENT, COMPRESSION

GMDN Terms

Code Name
62924 Surgical tissue compression device

Identifiers

Type ID
Primary 00192896032057

Customer Contacts