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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
Saliva collection mouthpiece IVD FDA UDI
Device Name
Saliva Collection Kits FDA UDI
Model / Reference
1 set/bag FDA UDI
Description
Saliva Collection Kits FDA UDI

Identifiers

Primary DI / UDI-DI
06974669350353 FDA UDI
FDA Product Code
EFN FDA UDI
GMDN Term
Saliva collection mouthpiece IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6050 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: Saliva collection mouthpiece IVD

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 Saliva collection mouthpiece IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 608b0e7a-6598-4363-8320-004b455dda08 33 fields · synced May 30, 2026