Insyte Autoguard BC Pro 392523

GUDID 30382903925231

Peripheral intravenous cannula

Primary Device ID	30382903925231
NIH Device Record Key	f022d9b2-a105-4b5c-9c50-b79dd625ca0f
Commercial Distribution Status	In Commercial Distribution
Brand Name	Insyte Autoguard BC Pro
Version Model Number	392523
Catalog Number	392523
Company DUNS	124987988
Company Name	BECTON, DICKINSON AND COMPANY
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	MR Conditional
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

Special Storage Condition, Specify	Between 0 and 0 *Room Temperature
Special Storage Condition, Specify	Between 0 and 0 *Room Temperature
Special Storage Condition, Specify	Between 0 and 0 *Room Temperature
Special Storage Condition, Specify	Between 0 and 0 *Room Temperature
Special Storage Condition, Specify	Between 0 and 0 *Room Temperature
Special Storage Condition, Specify	Between 0 and 0 *Room Temperature
Special Storage Condition, Specify	Between 0 and 0 *Room Temperature
Special Storage Condition, Specify	Between 0 and 0 *Room Temperature
Special Storage Condition, Specify	Between 0 and 0 *Room Temperature
Special Storage Condition, Specify	Between 0 and 0 *Room Temperature
Special Storage Condition, Specify	Between 0 and 0 *Room Temperature

Device Issuing Agency	Device ID
GS1	00382903925230 [Primary]
GS1	30382903925231 [Package] Contains: 00382903925230 Package: Shelfpack [50 Units] In Commercial Distribution
GS1	50382903925235 [Package] Package: Case [4 Units] In Commercial Distribution

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

Steralize Prior To Use	false
Device Is Sterile	true