FDA UDI In Commercial Distribution 🇺🇸 United States

Beurer

DI: 00850018808705 · Model: EM 49 · BEURER NORTH AMERICA, L.P.
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Beurer
Primary DI
00850018808705
Version / Model
EM 49
Catalog Number
662.78
Company Name
BEURER NORTH AMERICA, L.P.
Labeler DUNS
078497467
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-20
Public Version
1
Public Version Date
2023-10-30
Public Version Status
New
Public Device Record Key
6e0c46c1-94b8-4993-bcf7-53e9b1dee0cc

Device Description

Digital EMS/TENS Unit

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
No
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
No

Product Codes

Code Name
NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter
NGX Stimulator, Muscle, Powered, For Muscle Conditioning

GMDN Terms

Code Name
46573 Physical therapy transcutaneous neuromuscular electrical stimulation system

Identifiers

Type ID
Package 10850018808702
Primary 00850018808705
Package 20850018808709

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K190347 000