← Back to catalogue

Trolley

FDA UDI

Class II (US FDA UDI)

by Shenzhen Yingzhi Technology Co., Ltd.

Identity

Trade Name
Trolley FDA UDI
Generic Name
Electromechanical device/system transport trolley FDA UDI
Model / Reference
M1 FDA UDI

Identifiers

Primary DI / UDI-DI
06971538580323 FDA UDI
510(k) Number
K230735 FDA UDI
FDA Product Code
OBP FDA UDI
GMDN Term
Electromechanical device/system transport trolley FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5805 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

Category: Electromechanical device/system transport trolley

Trolley by Shenzhen Yingzhi Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electromechanical device/system transport trolley.

Cleared under the same submission

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 0ef41004-e4a5-463a-95bf-a50e45b61e16 33 fields · synced Jun 6, 2026