Nebulizer, Hand Held 166300

GUDID 00817081026412

Nebulizer, Hand Held

A-M SYSTEMS, LLC

Nebulizing system delivery set, single-use
Primary Device ID00817081026412
NIH Device Record Key25598adb-f19e-4126-9da6-93f2780d7d1c
Commercial Distribution StatusIn Commercial Distribution
Brand NameNebulizer, Hand Held
Version Model NumberNebulizer, Hand Held - 166300
Catalog Number166300
Company DUNS020275145
Company NameA-M SYSTEMS, LLC
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 Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone3606838300
Emailsales@a-msystems.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100817081026405 [Primary]
GS100817081026412 [Package]
Contains: 00817081026405
Package: [50 Units]
In Commercial Distribution

FDA Product Code

EPNPump, Nebulizer, Manual

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-04-20
Device Publish Date2020-04-10

On-Brand Devices [Nebulizer, Hand Held]

00817081026436Nebulizer, Hand Held
00817081026412Nebulizer, Hand Held

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