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Hisense

FDA UDI

Class II (US FDA UDI)

by Qingdao Hisense Medical Equipment Co., Ltd.

Identity

Trade Name
Hisense FDA UDI
Generic Name
Image display unit, monochrome FDA UDI
Device Name
LCD Monitor FDA UDI
Model / Reference
HMD2G21S FDA UDI
Description
LCD Monitor FDA UDI

Identifiers

Primary DI / UDI-DI
06933741405343 FDA UDI
510(k) Number
K222132 FDA UDI
FDA Product Code
PGY FDA UDI
GMDN Term
Image display unit, monochrome FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.2050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Image display unit, monochrome

Hisense by Qingdao Hisense Medical Equipment Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Image display unit, monochrome.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Qingdao Hisense Medical Equipment Co., Ltd.

Sources (1)

  • FDA UDI 4716f531-98d4-4bc0-826e-d051fa96c0e7 34 fields · synced Jun 6, 2026