FDA UDI In Commercial Distribution 🇺🇸 United States

Brain Depressor

DI: 00192896102781 · Model: 412-787 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Brain Depressor
Primary DI
00192896102781
Version / Model
412-787
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-30
Public Version
1
Public Version Date
2020-07-08
Public Version Status
New
Public Device Record Key
cc61e812-8db8-42b2-a2d8-2b5caa796422

Device Description

Cushing Brain Depressor Double-Ended

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
GAF SPATULA, SURGICAL, GENERAL & PLASTIC SURGERY

GMDN Terms

Code Name
14367 Vessel depressor

Identifiers

Type ID
Primary 00192896102781

Customer Contacts

Device Sizes

Type Value Unit Text
Length 6.75 Inch