Delta Fly®

GUDID 58032248369127

Venous butterfly needle/set

Primary Device ID	58032248369127
NIH Device Record Key	6cfe45e5-571e-4e3f-a7ff-58d2d30a2d00
Commercial Distribution Status	In Commercial Distribution
Brand Name	Delta Fly®
Version Model Number	3691222
Company DUNS	444776777
Company Name	DELTA MED SPA
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	true
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	true
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	08032248369122 [Primary]
GS1	38032248369123 [Package] Contains: 08032248369122 Package: Box [60 Units] In Commercial Distribution
GS1	58032248369127 [Package] Contains: 38032248369123 Package: Case [20 Units] In Commercial Distribution

FPA	Set, Administration, Intravascular

Steralize Prior To Use	false
Device Is Sterile	true

58032248369127	Delta Fly Micro Bore Winged Safety Needle
58032248369028	Delta Fly Micro Bore F20 Winged Safety Needle
58032248368526	Delta Fly Micro Bore F20 Winged Safety Needle
58032248368168	Delta Fly Micro Bore Winged Safety Needle

Mark Image Registration \| Serial	Company Trademark Application Date
DELTA FLY 76237956 not registered Dead/Abandoned	DELTA CORPORATE IDENTITY, INC. 2001-04-03