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Xukang

FDA UDI

Class I (US FDA UDI)

by Hengshui Xukang Medical Appliances Co., Ltd

Identity

Trade Name
Xukang FDA UDI
Generic Name
General-purpose patient lifting system sling/harness FDA UDI
Model / Reference
One Size FDA UDI

Identifiers

Primary DI / UDI-DI
06974518523143 FDA UDI
FDA Product Code
ILI FDA UDI
GMDN Term
General-purpose patient lifting system sling/harness FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3640 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General-purpose patient lifting system sling/harness

Xukang by Hengshui Xukang Medical Appliances Co., Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose patient lifting system sling/harness.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c1e207da-e5cc-4c8b-a4c3-c8411c2e1e59 32 fields · synced May 30, 2026