Insyte Autoguard BC Pro 392647

GUDID 30382903926474

Peripheral intravenous cannula

Primary Device ID	30382903926474
NIH Device Record Key	c634ed81-59f1-45df-830a-b855f187ff40
Commercial Distribution Status	In Commercial Distribution
Brand Name	Insyte Autoguard BC Pro
Version Model Number	392647
Catalog Number	392647
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	true
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

Device Issuing Agency	Device ID
GS1	00382903926473 [Primary]
GS1	30382903926474 [Package] Contains: 00382903926473 Package: Shelfpack [50 Units] In Commercial Distribution
GS1	50382903926478 [Package] Contains: 00382903926473 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