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Haier Biomedical

FDA UDI

Class I (US FDA UDI)

by Qingdao Haier Biomedical Technology Co., Ltd.

Identity

Trade Name
Haier Biomedical FDA UDI
Generic Name
Carbon dioxide laboratory incubator FDA UDI
Device Name
Carbon dioxide laboratory incubator FDA UDI
Model / Reference
HCP-160B FDA UDI
Description
Carbon dioxide laboratory incubator FDA UDI

Identifiers

Catalog Number
HCP-160B FDA UDI
Primary DI / UDI-DI
06974440221018 FDA UDI
FDA Product Code
JTQ FDA UDI
GMDN Term
Carbon dioxide laboratory incubator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2540 FDA UDI
Commercial Distribution
Not 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Haier Biomedical by Qingdao Haier Biomedical Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8054cfad-b8af-426d-9a44-a1d9da59e187 35 fields · synced May 30, 2026