FDA UDI In Commercial Distribution 🇺🇸 United States

COBB CURETTE

DI: 00192896101869 · Model: 320-901 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
COBB CURETTE
Primary DI
00192896101869
Version / Model
320-901
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-18
Public Version
1
Public Version Date
2020-05-26
Public Version Status
New
Public Device Record Key
2e1bd8c7-1e01-426b-8592-2015ea3e133a

Device Description

Cobb Curette Straight Oval Cup

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
HTF CURETTE

GMDN Terms

Code Name
31335 Bone curette, reusable

Identifiers

Type ID
Primary 00192896101869

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Size 3
Length 11 Inch