FDA UDI In Commercial Distribution 🇺🇸 United States

BRUNS ARTHROSCOPIC CURETTE

DI: 00192896077836 · Model: 320-880 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BRUNS ARTHROSCOPIC CURETTE
Primary DI
00192896077836
Version / Model
320-880
Catalog Number
320-880
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-20
Public Version
2
Public Version Date
2019-05-07
Public Version Status
Update
Public Device Record Key
308ef4d5-b767-47cb-abee-70dab84586f0

Device Description

BRUNS ARTHROSCOPIC CURETTE SIZE 0000

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
HTF CURETTE

GMDN Terms

Code Name
31335 Bone curette, reusable

Identifiers

Type ID
Primary 00192896077836

Customer Contacts

Device Sizes

Type Value Unit Text
Length 9 Inch
Device Size Text, specify 3 Millimeter Tip