SUCTION TUBE N4451740

GUDID 04953170467233

OLYMPUS MEDICAL SYSTEMS CORP.

Endoscopic insufflation tubing set, reusable
Primary Device ID04953170467233
NIH Device Record Key94ed963c-4faf-4cfd-805e-c73012788c38
Commercial Distribution StatusIn Commercial Distribution
Brand NameSUCTION TUBE
Version Model NumberMAJ-591
Catalog NumberN4451740
Company DUNS711789789
Company NameOLYMPUS MEDICAL SYSTEMS CORP.
Device Count1
DM Exempttrue
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 Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS104953170467233 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HIFInsufflator, Laparoscopic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04953170467233]

Moist Heat or Steam Sterilization;Ethylene Oxide


[04953170467233]

Moist Heat or Steam Sterilization;Ethylene Oxide


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-03-06
Device Publish Date2025-02-26

On-Brand Devices [SUCTION TUBE]

04953170061325REUSABLE SUCTION TUBING FOR UHI
04953170026737"MB-721 SUCTION TUBE FOR LUS"
04953170467233MAJ-591

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.