KV-6 Suction Pump K10026148

GUDID 07612367052467

Suction Pump 071.0005-04

Medela AG

General-purpose suction system, line-powered General-purpose suction system, line-powered General-purpose suction system, line-powered Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump Surgical suction pump
Primary Device ID07612367052467
NIH Device Record Keye606d062-503a-4628-9930-ede3b15c41af
Commercial Distribution StatusIn Commercial Distribution
Brand NameKV-6 Suction Pump
Version Model Number200.5625
Catalog NumberK10026148
Company DUNS488293218
Company NameMedela AG
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
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
GS107612367044950 [Primary]
GS107612367044967 [Primary]
GS107612367044981 [Primary]
GS107612367052467 [Direct Marking]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

BTAPump, Portable, Aspiration (Manual Or Powered)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-10-03

On-Brand Devices [KV-6 Suction Pump]

07612367052467Suction Pump 071.0005-04
07612367044974Suction Pump 071.0005-03

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