MICROTOOLS (Polar Body Biopsy Pipette) - A non-invasive, single-use micro-manipulation - Arsci Inc.

Duns Number:241975256

Device Description: A non-invasive, single-use micro-manipulation pipette used in the laboratory to inject, de A non-invasive, single-use micro-manipulation pipette used in the laboratory to inject, denude, mobilize, remove, aspirate, incise, manipulate or separate cells for the duration of In-Vitro Fertilization (IVF), Assisted Reproductive Technologies (ART), and Reproductive Medicine (RM) procedures.The Polar Body Biopsy Pipette is to be used by qualified personnel during In-Vitro Fertilization (IVF) or Assisted Reproduction Technology (ART) procedures in vitro, for the aspiration of polar bodies from oocytes for pre-implantation genetic diagnosis (PGD) on the genetic material in the biopsied cell(s). Intended for one-time use.

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More Product Details

Catalog Number

-

Brand Name

MICROTOOLS (Polar Body Biopsy Pipette)

Version/Model Number

PB-35FP01

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)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K102480,K102480

Product Code Details

Product Code

MQH

Product Code Name

Microtools, Assisted Reproduction (Pipettes)

Device Record Status

Public Device Record Key

adfce139-3bad-4e0c-8100-1cbbaf891627

Public Version Date

October 17, 2022

Public Version Number

1

DI Record Publish Date

October 07, 2022

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"ARSCI INC." Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 45