Microlife

GUDID 10642632472007

MICROLIFE USA, INC.

Nebulizing system, non-heated Nebulizing system, non-heated Nebulizing system, non-heated
Primary Device ID10642632472007
NIH Device Record Key45304925-c3b8-43a3-8fe0-a9ed15b7dd4f
Commercial Distribution StatusIn Commercial Distribution
Brand NameMicrolife
Version Model NumberNEB200
Company DUNS176387785
Company NameMICROLIFE USA, INC.
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 Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100642632472000 [Primary]
GS100642632472000 [Primary]
GS100642632472000 [Primary]
GS110642632472007 [Package]
Contains: 00642632472000
Package: [6 Units]
In Commercial Distribution
GS110642632472007 [Package]
Contains: 00642632472000
Package: [6 Units]
In Commercial Distribution
GS110642632472007 [Package]
Contains: 00642632472000
Package: [6 Units]
In Commercial Distribution

FDA Product Code

CAFNebulizer (Direct Patient Interface)
CAFNebulizer (Direct Patient Interface)
CAFNebulizer (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 Date2020-05-21
Device Publish Date2020-05-13

On-Brand Devices [Microlife]

10642632732002PF100
10642632410092BP3AQ1-1
10642632410016BP3MC1-PC
00642632393510BP3GX1-5A
00642632393008BP3GX1-5N
10642632392008BP3GQ1-3P
10642632391001BP3GR1-3P 
10642632351050BP3MY1-1P
16970388169129Model: b990655-2 Office ABI
16970388160102Office AFIB
26970388160086Model: b980310-3
16970388160072b980210-3 03 Watch BP
20642632900019BP3GY1-2N
10642632472007NEB200

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