MICROTOOLS (Biopsy Pipette)

FDA UDI

Class II (US FDA UDI)

by Arsci Inc.

Identity

Trade Name: MICROTOOLS (Biopsy Pipette) FDA UDI
Generic Name: Assisted reproduction microtool FDA UDI
Device Name: 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 Biopsy Pipette is to be used by qualified personnel during In-Vitro Fertilization (IVF) or Assisted Reproduction Technology (ART) procedures in vitro, to aspirate or remove blastomere(s) from a developing embryo for pre-implantation genetic diagnosis (PGD) on the genetic material in the biopsied cell(s). Intended for one-time use. FDA UDI
Model / Reference: B-35FP01 FDA UDI
Description: 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 Biopsy Pipette is to be used by qualified personnel during In-Vitro Fertilization (IVF) or Assisted Reproduction Technology (ART) procedures in vitro, to aspirate or remove blastomere(s) from a developing embryo for pre-implantation genetic diagnosis (PGD) on the genetic material in the biopsied cell(s). Intended for one-time use. FDA UDI

Identifiers

Primary DI / UDI-DI: 07540268000624 FDA UDI
510(k) Number: K102480 FDA UDI
FDA Product Code: MQH FDA UDI
GMDN Term: Assisted reproduction microtool FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 884.6130 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Assisted reproduction microtool

MICROTOOLS (Biopsy Pipette) by Arsci Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Arsci Inc.

Sources (1)

FDA UDI e88eb9a0-2249-4109-939a-dad980d9d0ed 35 fields · synced May 30, 2026