← Back to catalogue

Ningbo Youhuan Automation Technology Co., Ltd.

FDA UDI

Class II (US FDA UDI)

by Ningbo Youhuan Automation Technology Co., Ltd

Identity

Trade Name
NINGBO YOUHUAN AUTOMATION TECHNOLOGY CO., LTD. FDA UDI
Generic Name
Electric-motor-driven wheelchair, occupant-controlled FDA UDI
Model / Reference
YH-E7001 FDA UDI

Identifiers

Primary DI / UDI-DI
06975028636538 FDA UDI
510(k) Number
K240638 FDA UDI
FDA Product Code
ITI FDA UDI
GMDN Term
Electric-motor-driven wheelchair, occupant-controlled FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.3860 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Ningbo Youhuan Automation Technology Co., Ltd. by Ningbo Youhuan Automation Technology Co., Ltd — Class II — FDA UDI — listed in FDA GUDID

Cleared under the same submission

K240638 also covers:

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

Manufacturer
Ningbo Youhuan Automation Technology Co., Ltd

Sources (1)

  • FDA UDI 00b9299c-ba2d-4579-8285-c42de2f6f2cc 34 fields · synced May 30, 2026