CADD

GUDID 10610586025181

Mechanical pipette

Primary Device ID	10610586025181
NIH Device Record Key	76eab9a8-82d6-4750-8453-b9e7cec821e2
Commercial Distribution Discontinuation	2019-08-13
Commercial Distribution Status	Not in Commercial Distribution
Brand Name	CADD
Version Model Number	21-4653-24
Company DUNS	106712748
Company Name	SMITHS MEDICAL MD, 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	true
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	10610586025181 [Primary]

FOZ	Catheter,intravascular,therapeutic,short-term less than 30 days

Steralize Prior To Use	false
Device Is Sterile	true

Mark Image Registration \| Serial	Company Trademark Application Date
CADD 85113149 4025048 Dead/Cancelled	Smiths Medical ASD, Inc. 2010-08-23
CADD 78847519 3201977 Live/Registered	SMITHS MEDICAL ASD, INC. 2006-03-28
CADD 75656568 2554554 Dead/Cancelled	NOBEL BIOCARE AB 1999-03-08
CADD 73751005 1547216 Live/Registered	PHARMACIA DELTEC, INC. 1988-09-07
CADD 73661271 1686787 Dead/Cancelled	AUDIO ANALYSTS INC. 1987-05-18
CADD 73062204 1070788 Dead/Cancelled	Ready Stamping System Inc. 1975-09-05