FDA UDI In Commercial Distribution 🇺🇸 United States

FINGER GONIOMETER

DI: 00192896032224 · Model: 350-915 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FINGER GONIOMETER
Primary DI
00192896032224
Version / Model
350-915
Catalog Number
350-915
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-13
Public Version
1
Public Version Date
2018-10-15
Public Version Status
New
Public Device Record Key
30b51361-557e-4edc-9b25-f7f6852e557f

Device Description

FINGER GONIOMETER

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
KQW Goniometer, nonpowered

GMDN Terms

Code Name
33651 Manual goniometer

Identifiers

Type ID
Primary 00192896032224

Customer Contacts

Device Sizes

Type Value Unit Text
Length 5.75 Inch