BKG

GUDID 10810011730554

Autoinjector needle

Primary Device ID	10810011730554
NIH Device Record Key	912afa7e-4d7b-4c97-b732-3cc17ceeb549
Commercial Distribution Status	In Commercial Distribution
Brand Name	BKG
Version Model Number	Ordinary Type
Company DUNS	421272490
Company Name	Tianjin Huahong Technology Co., Ltd.
Device Count	100
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	true
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	true

Device Issuing Agency	Device ID
GS1	00810011730557 [Primary]
GS1	10810011730554 [Package] Contains: 00810011730557 Package: case [5000 Units] In Commercial Distribution
GS1	50810011730552 [Unit of Use]

FMI	Needle, Hypodermic, Single Lumen

Steralize Prior To Use	false
Device Is Sterile	true