Insufflator 50L

GUDID 04056702007218

W.O.M. World of Medicine GmbH

Laparoscopic insufflator
Primary Device ID04056702007218
NIH Device Record Keyde83c6a0-6c9f-42df-bc4c-0f3168899061
Commercial Distribution StatusIn Commercial Distribution
Brand NameInsufflator 50L
Version Model NumberFM134
Company DUNS316305242
Company NameW.O.M. World of Medicine GmbH
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 Batchfalse
Serial Numbertrue
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
GS104056702007218 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HIFInsufflator, Laparoscopic

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-07-02
Device Publish Date2019-06-24

On-Brand Devices [Insufflator 50L]

04056702005771FM134
04056702003227FM134
04056702007218FM134
04056702008895ZEOSINSUFF

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