FDA UDI In Commercial Distribution 🇺🇸 United States

TetraSens

DI: 07350012440022 · Model: TetraSens · Senzime AB (Publ.)
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
TetraSens
Primary DI
07350012440022
Version / Model
TetraSens
Catalog Number
SEN 2002
Company Name
Senzime AB (Publ.)
Labeler DUNS
559976316
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-23
Public Version
4
Public Version Date
2023-09-25
Public Version Status
Update
Public Device Record Key
9efb9cdb-7124-4fa4-8993-61ef30caa484

Device Description

TetraSens TetraGraph Electrode

Device Characteristics

Single Use
Yes
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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KOI Stimulator, Nerve, Peripheral, Electric

GMDN Terms

Code Name
35722 Block-monitoring peripheral nerve electrical stimulation system

Identifiers

Type ID
Package 07350012440039
Primary 07350012440022

Customer Contacts

Phone
800-213-1324