← 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
Face splash shield, single-use FDA UDI
Device Name
Medical Face Shield FDA UDI
Model / Reference
5 pcs FDA UDI
Description
Medical Face Shield FDA UDI

Identifiers

Primary DI / UDI-DI
06974669350193 FDA UDI
FDA Product Code
KPY FDA UDI
GMDN Term
Face splash shield, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.6500 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: Face splash shield, single-use

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 Face splash shield, single-use.

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 59258c2a-71c6-4cf2-a33f-38fc8ce88996 33 fields · synced Jun 8, 2026