Sterilance Press4 Pressure Activated Safety Lancet - Sterilance Press4 Pressure Activated Safety - SteriLance Medical (Suzhou) Inc.

Duns Number:421141183

Device Description: Sterilance Press4 Pressure Activated Safety Lancet,28G 1.8mm,100Lancets/box

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More Product Details

Catalog Number

-

Brand Name

Sterilance Press4 Pressure Activated Safety Lancet

Version/Model Number

05-082818

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"

-

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

Yes

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

fbd408d1-733e-4991-972e-92afcf320399

Public Version Date

November 25, 2020

Public Version Number

1

DI Record Publish Date

November 17, 2020

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"STERILANCE MEDICAL (SUZHOU) INC." Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 19