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Mdhc

FDA UDI

Class I (US FDA UDI)

by MDHC Life Technologies (Kunshan) Co., LTD.

Identity

Trade Name
MDHC FDA UDI
Generic Name
Sperm filtration system FDA UDI
Device Name
Filtration Systems FDA UDI
Model / Reference
12 pcs/Case FDA UDI
Description
Filtration Systems FDA UDI

Identifiers

Primary DI / UDI-DI
06974669350339 FDA UDI
FDA Product Code
KET FDA UDI
GMDN Term
Sperm filtration system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3010 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Sperm filtration system

Mdhc by MDHC Life Technologies (Kunshan) Co., LTD. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sperm filtration system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
MDHC Life Technologies (Kunshan) Co., LTD.

Sources (1)

  • FDA UDI ecd54d2c-dae3-4e7f-bffe-ccab4e7bb838 33 fields · synced May 29, 2026