FDA UDI In Commercial Distribution 🇺🇸 United States

TENS 212

DI: 00816864020135 · Model: ME 212 · METTLER ELECTRONICS CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TENS 212
Primary DI
00816864020135
Version / Model
ME 212
Catalog Number
ME 212
Company Name
METTLER ELECTRONICS CORP.
Labeler DUNS
008513913
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-15
Public Version
8
Public Version Date
2023-06-02
Public Version Status
Update
Public Device Record Key
03a3a384-6119-40c8-8f77-ea114e137db2

Device Description

Two-channel digial TENS device with LCD display

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
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GZJ STIMULATOR, NERVE, TRANSCUTANEOUS, FOR PAIN RELIEF

GMDN Terms

Code Name
46573 Physical therapy transcutaneous neuromuscular electrical stimulation system

Identifiers

Type ID
Primary 00816864020135

Customer Contacts

Phone
+1(714)533-2221 ext. 319

Premarket Submissions

Submission Number Supplement Number
K032720 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Battery Included
Weight 140 Gram

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
No