Micro well group culture dish, 9-well - The Micro Well Group Culture Dish is designed for - Vitrolife A/S

Duns Number:308547608

Device Description: The Micro Well Group Culture Dish is designed for efficient embryo handling and culture. T The Micro Well Group Culture Dish is designed for efficient embryo handling and culture. The nine (9) microwells are intended for embryo culture at all stages. The wells are intended to hold one embryo each. The area surrounding the wells can contain a sufficient amount of culture medium for all embryos, thereby allowing efficient culture setup and handling. The individual microwells allows individual evaluation of each embryo during group culture.The Micro Well Group Culture Dish is constructed of polysterene and is non-pyrogenic. The raw material has passed mouse embryo testing prior to production and the dish is sterilised by beta irradiation. Sterility Assurance level 10-6 (SAL 10-6).Indications for Use / Intended Use:For in vitro fertilisation, handling and embryo culture. It may be used for culturing of embryos using drop culture.

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More Product Details

Catalog Number

16604

Brand Name

Micro well group culture dish, 9-well

Version/Model Number

16604

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K150756,K150756

Product Code Details

Product Code

MQK

Product Code Name

Labware, Assisted Reproduction

Device Record Status

Public Device Record Key

b3281f13-59f6-4a78-ae9b-df66bb48c615

Public Version Date

March 10, 2021

Public Version Number

4

DI Record Publish Date

September 21, 2017

Additional Identifiers

Package DI Number

15712714666046

Quantity per Package

10

Contains DI Package

05712714666049

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Card board box

"VITROLIFE A/S" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 1
2 A medical device with a moderate to high risk that requires special controls. 2