ConMed Inflation Device 96282

GUDID 00653405052350

Catheter/overtube balloon inflator, single-use

Primary Device ID	00653405052350
NIH Device Record Key	5f9e9295-9e0c-4f91-a926-6ff718045bdf
Commercial Distribution Status	In Commercial Distribution
Brand Name	ConMed Inflation Device
Version Model Number	QL® 6015
Catalog Number	96282
Company DUNS	047571476
Company Name	ATRION MEDICAL PRODUCTS, INC.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00653405052350 [Primary]

KOE	Dilator, Urethral

Steralize Prior To Use	false
Device Is Sterile	true

10653405052357	Inflation Device: 60mL, 15atm
00653405052350	Inflation Device: 60mL, 15atm