← Back to catalogue

Mdhc

FDA UDI

Class I (US FDA UDI)

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

Identity

Trade Name
MDHC FDA UDI
Generic Name
Cervical cytology microscopy slide IVD FDA UDI
Device Name
Cell Culture Slide FDA UDI
Model / Reference
6 pcs/box FDA UDI
Description
Cell Culture Slide FDA UDI

Identifiers

Primary DI / UDI-DI
06974669350315 FDA UDI
FDA Product Code
KIY FDA UDI
GMDN Term
Cervical cytology microscopy slide IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.2240 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: Cervical cytology microscopy slide 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 Cervical cytology microscopy slide IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI cb350e20-1951-4f3c-a446-02b110a5a2ea 33 fields · synced May 31, 2026