Acti-Lance, safety lancet - Safety lancets are sterile, single use medical - HTL STREFA S A

Duns Number:422528088

Device Description: Safety lancets are sterile, single use medical devices intended for capillary blood sampli Safety lancets are sterile, single use medical devices intended for capillary blood sampling. Intended users are healthcare professionals and lay users.

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More Product Details

Catalog Number

7321

Brand Name

Acti-Lance, safety lancet

Version/Model Number

Lite, 28G

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)

-

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

FMK

Product Code Name

Lancet, Blood

Device Record Status

Public Device Record Key

fd7c01f4-a32d-48dc-bbb8-27a04b288189

Public Version Date

May 25, 2020

Public Version Number

1

DI Record Publish Date

May 17, 2020

Additional Identifiers

Package DI Number

15907996096890

Quantity per Package

24

Contains DI Package

05907996096893

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

shipper

"HTL STREFA S A" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 2