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Im-Hd1tvm

FDA UDI

Class II (US FDA UDI)

by Narishige Lifemed Co., Ltd.

Identity

Trade Name
IM-HD1TVM FDA UDI
Generic Name
Assisted reproduction electromechanical micromanipulator FDA UDI
Device Name
Assisted Reproduction Microinjector FDA UDI
Model / Reference
IM-HD1TVM Pneumatic Microinjector FDA UDI
Description
Assisted Reproduction Microinjector FDA UDI

Identifiers

Primary DI / UDI-DI
04589818020128 FDA UDI
FDA Product Code
MQJ FDA UDI
GMDN Term
Assisted reproduction electromechanical micromanipulator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.6150 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Assisted reproduction electromechanical micromanipulator

Im-Hd1tvm by Narishige Lifemed Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Assisted reproduction electromechanical micromanipulator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Narishige Lifemed Co., Ltd.

Sources (1)

  • FDA UDI a6f4dba2-5435-4a47-a9d6-a64431567839 34 fields · synced May 30, 2026