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XinjingProWellness™

FDA UDI

Class I (US FDA UDI)

by Tianjin Newtrans Technology Development

Identity

Trade Name
XinjingProWellness™ FDA UDI
Generic Name
Airway device cleaning utensil, noninvasive, reusable FDA UDI
Model / Reference
1003-B FDA UDI

Identifiers

Primary DI / UDI-DI
16973881680047 FDA UDI
FDA Product Code
EPE FDA UDI
GMDN Term
Airway device cleaning utensil, noninvasive, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5795 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Airway device cleaning utensil, noninvasive, reusable

XinjingProWellness™ by Tianjin Newtrans Technology Development — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Airway device cleaning utensil, noninvasive, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e0a00771-d571-4d4e-87b3-ece574050367 32 fields · synced May 30, 2026