BioMed 2000 XL KBXL

GUDID 00857771003149

BIOMEDICAL LIFE SYSTEMS, INC.

Analgesic transcutaneous electrical nerve stimulation system
Primary Device ID00857771003149
NIH Device Record Key62b0d279-7932-4f0d-a154-35a025fd4000
Commercial Distribution Discontinuation2017-01-04
Commercial Distribution StatusNot in Commercial Distribution
Brand NameBioMed 2000 XL
Version Model Number2000XL
Catalog NumberKBXL
Company DUNS116956807
Company NameBIOMEDICAL LIFE SYSTEMS, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone7607275600
Emailinformation@bmls.com

Device Dimensions

Height6 Inch
Height6 Inch
Height6 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100857771003149 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GZJStimulator, Nerve, Transcutaneous, For Pain Relief

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-10-23
Device Publish Date2016-09-23

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