Medline - NEEDLE,HYPODERM,SAFETY, 23GX1" - MEDLINE INDUSTRIES, INC.

Duns Number:025460908

Device Description: NEEDLE,HYPODERM,SAFETY, 23GX1"

Want to know more about this Product? Request more information now!


More Product Details

Catalog Number

SYRS100235

Brand Name

Medline

Version/Model Number

SYRS100235

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

Yes

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code Details

Product Code

FMI

Product Code Name

Needle, hypodermic, single lumen

Device Record Status

Public Device Record Key

12734660-e33b-49ea-aec4-9d7691d0613f

Public Version Date

December 22, 2020

Public Version Number

1

DI Record Publish Date

December 14, 2020

Additional Identifiers

Package DI Number

30888277221233

Quantity per Package

100

Contains DI Package

10888277221239

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX

"MEDLINE INDUSTRIES, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 38540
2 A medical device with a moderate to high risk that requires special controls. 85094
3 A medical device with high risk that requires premarket approval 2
U Unclassified 7