Duns Number:718296825
Device Description: Box of 30 Sterile Lancets 30 Gauge
Catalog Number
OTDP Lancet 30g 30 US
Brand Name
OneTouch Delica Plus Lancet
Version/Model Number
02419901
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
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
K221546,K221546,K221546
Product Code
QRK
Product Code Name
Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature
Public Device Record Key
412cd8ed-4bbd-4284-b0ea-6ec234dacaf4
Public Version Date
September 28, 2022
Public Version Number
2
DI Record Publish Date
November 18, 2020
Package DI Number
20812608030211
Quantity per Package
240
Contains DI Package
00812608030217
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Cardboard box
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 1 |