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Mdhc

FDA UDI

Class II (US FDA UDI)

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

Identity

Trade Name
MDHC FDA UDI
Generic Name
Assay container IVD, single-use FDA UDI
Device Name
Reagent Reservoir FDA UDI
Model / Reference
5 pcs/bag FDA UDI
Description
Reagent Reservoir FDA UDI

Identifiers

Primary DI / UDI-DI
06974669350261 FDA UDI
FDA Product Code
PTN FDA UDI
GMDN Term
Assay container IVD, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4400 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: Assay container IVD, single-use

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

Similar devices

Also classified as Assay container IVD, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 212b1fb4-d69f-4ee2-ab54-56f61d47b73c 33 fields · synced May 30, 2026