Filter Line 0600-2010-000

GUDID 10817984010089

Endoscopic insufflation tubing set, single-use

Primary Device ID	10817984010089
NIH Device Record Key	39ef42b4-3c28-4199-8e39-95a4f678e38f
Commercial Distribution Discontinuation	2020-01-10
Commercial Distribution Status	Not in Commercial Distribution
Brand Name	Filter Line
Version Model Number	0600-2010-000
Catalog Number	0600-2010-000
Company DUNS	606939072
Company Name	MECTRA LABS, 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

Handling Environment Temperature	Between 20 Degrees Fahrenheit and 115 Degrees Fahrenheit
Handling Environment Temperature	Between 20 Degrees Fahrenheit and 115 Degrees Fahrenheit
Handling Environment Temperature	Between 20 Degrees Fahrenheit and 115 Degrees Fahrenheit
Handling Environment Temperature	Between 20 Degrees Fahrenheit and 115 Degrees Fahrenheit
Handling Environment Temperature	Between 20 Degrees Fahrenheit and 115 Degrees Fahrenheit
Handling Environment Temperature	Between 20 Degrees Fahrenheit and 115 Degrees Fahrenheit
Handling Environment Temperature	Between 20 Degrees Fahrenheit and 115 Degrees Fahrenheit
Handling Environment Temperature	Between 20 Degrees Fahrenheit and 115 Degrees Fahrenheit

Device Issuing Agency	Device ID
GS1	00817984010082 [Primary]
GS1	10817984010089 [Package] Contains: 00817984010082 Package: Inner pack [10 Units] Discontinued: 2020-01-10 Not in Commercial Distribution

HIF	INSUFFLATOR, LAPAROSCOPIC

Steralize Prior To Use	false
Device Is Sterile	true