Coude Dual Lumen Catheter 7F

GUDID 10627825000250

Urodynamic manometric catheter, non-electronic

Primary Device ID	10627825000250
NIH Device Record Key	0c83618a-0bdc-42af-9e76-7b132351b851
Commercial Distribution Status	In Commercial Distribution
Brand Name	Coude Dual Lumen Catheter 7F
Version Model Number	CDLC-7D
Company DUNS	203383526
Company Name	Laborie Medical Technologies Canada ULC
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	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	true
RX Perscription	false
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00627825000253 [Primary]
GS1	10627825000250 [Package] Contains: 00627825000253 Package: [10 Units] In Commercial Distribution
GS1	20627825000257 [Package] Package: [240 Units] In Commercial Distribution

FEN	DEVICE, CYSTOMETRIC, HYDRAULIC

Steralize Prior To Use	true
Device Is Sterile	true

[10627825000250]

Ethylene Oxide

[10627825000250]

Ethylene Oxide