Optichamber Diamond 166401

GUDID 00817081026597

Valved Holding Chamber, Optichamber Diamond

A-M SYSTEMS, LLC

Medicine chamber spacer, reusable
Primary Device ID00817081026597
NIH Device Record Key18ae3d01-8e03-4bde-ba0e-9713c793e076
Commercial Distribution StatusIn Commercial Distribution
Brand NameOptichamber Diamond
Version Model NumberOptichamber Diamond - 166401
Catalog Number166401
Company DUNS020275145
Company NameA-M SYSTEMS, LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
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-Countertrue

Customer Support Contacts

Phone3606838300
Emailsales@a-msystems.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100817081026597 [Primary]

FDA Product Code

NVPHolding Chambers, Direct Patient Interface

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-04-21
Device Publish Date2020-04-13

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