RTube 2501

GUDID 00860009311602

RTube Single-use disposable exhaled breath condensate collector.

Respiratory Research Inc

Exhaled-gas sample collector, non-electronic Exhaled-gas sample collector, non-electronic Exhaled-gas sample collector, non-electronic Exhaled-gas sample collector, non-electronic Exhaled-gas sample collector, non-electronic Exhaled-gas sample collector, non-electronic Exhaled-gas sample collector, non-electronic Exhaled-gas sample collector, non-electronic Exhaled-gas sample collector, non-electronic Exhaled-gas sample collector, non-electronic Exhaled-gas sample collector, non-electronic Exhaled-gas sample collector, non-electronic Exhaled-gas sample collector, non-electronic Exhaled-gas sample collector, non-electronic Exhaled-gas sample collector, non-electronic Exhaled-gas sample collector, non-electronic Exhaled-gas sample collector, non-electronic

Primary Device ID	00860009311602
NIH Device Record Key	763f535d-987f-4aeb-8237-6df2dae2d558
Commercial Distribution Status	In Commercial Distribution
Brand Name	RTube
Version Model Number	2501
Catalog Number	2501
Company DUNS	157929535
Company Name	Respiratory Research Inc
Device Count	1
DM Exempt	false
Pre-market Exempt	true
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	true
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860009311602 [Primary]

FDA Product Code

KGK	Gas, Collecting Vessel

Sterilization

Steralize Prior To Use	false
Device Is Sterile	false

Device Entry Metadata

Public Version Status	New
Device Record Status	Published
Public Version Number	1
Public Version Date	2023-11-29
Device Publish Date	2023-11-21