AMC&E

GUDID 30817357020831

AMC&E 5-lead DIN to Pinch Telemetry Leadset

HYGIA HEALTH SERVICES, INC.

Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed Electrocardiographic lead set, reprocessed
Primary Device ID30817357020831
NIH Device Record Keya21c62bd-b1e5-4602-b766-bb55f271f16d
Commercial Distribution Discontinuation2019-07-10
Commercial Distribution StatusNot in Commercial Distribution
Brand NameAMC&E
Version Model NumberLW-309DS50/5AT
Company DUNS177939027
Company NameHYGIA HEALTH SERVICES, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS110817357020837 [Primary]
GS130817357020831 [Package]
Contains: 10817357020837
Package: Box [25 Units]
Discontinued: 2021-03-19
Not in Commercial Distribution

FDA Product Code

IKDCable, Electrode

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2021-03-19
Device Publish Date2016-09-30

On-Brand Devices [AMC&E]

30817357021241AMC&E 5-Lead Grouped Set, Pinch (Grabber) to Multi-Link® Shielded Disposable, 50in.
30817357020831AMC&E 5-lead DIN to Pinch Telemetry Leadset
30817357020572AMC&E 3-lead DIN to Pinch Leadset
30817357020480AMC&E 5-lead DIN to Pinch Leadset

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.