NIPRO SAFETOUCH™ II SAFETY FISTULA NEEDLE FS+162530BCR

GUDID 10383790000137

Haemodialysis needle Haemodialysis needle

Primary Device ID	10383790000137
NIH Device Record Key	c4542094-4697-4420-a1b9-52922cb598d3
Commercial Distribution Status	In Commercial Distribution
Brand Name	NIPRO SAFETOUCH™ II SAFETY FISTULA NEEDLE
Version Model Number	16GX1" HTC-30W
Catalog Number	FS+162530BCR
Company DUNS	797372554
Company Name	NIPRO MEDICAL CORPORATION
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	false
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00383790000130 [Primary]
GS1	10383790000137 [Package] Contains: 00383790000130 Package: Carton [50 Units] In Commercial Distribution
GS1	40383790000138 [Package] Package: Case [10 Units] In Commercial Distribution

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

Steralize Prior To Use	false
Device Is Sterile	true