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RI Pipettes

FDA UDI

Class II (US FDA UDI)

by Research Instruments , Ltd.

Identity

Trade Name
RI Pipettes FDA UDI
Generic Name
Assisted reproduction microtool FDA UDI
Device Name
Assisted Reproduction Microtools (Pipettes) FDA UDI
Model / Reference
Flat Biopsy FDA UDI
Description
Assisted Reproduction Microtools (Pipettes) FDA UDI

Identifiers

Catalog Number
7-71-35FB15/20 FDA UDI
Primary DI / UDI-DI
05060170182758 FDA UDI
510(k) Number
K133257 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

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Lumen/Inner Diameter — 35 Micrometer FDA UDI

Category: Assisted reproduction microtool

RI Pipettes by Research Instruments , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Assisted reproduction microtool.

Cleared under the same submission

K133257 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Research Instruments , Ltd.

Sources (1)

  • FDA UDI a366691a-0633-4d0f-97bc-d8ebf2a79126 38 fields · synced May 30, 2026