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VR Medical Technology Co., Ltd.

FDA UDI

Class I (US FDA UDI)

by Vr Medical Technology

Identity

Trade Name
VR Medical Technology Co., Ltd. FDA UDI
Generic Name
Airway suction catheter FDA UDI
Device Name
Closed suction System ,VR041605 FDA UDI
Model / Reference
Closed suction System FDA UDI
Description
Closed suction System ,VR041605 FDA UDI

Identifiers

Catalog Number
VR041605 FDA UDI
Primary DI / UDI-DI
16959180720479 FDA UDI
FDA Product Code
BSY FDA UDI
GMDN Term
Airway suction catheter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6810 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Airway suction catheter

VR Medical Technology Co., Ltd. by Vr Medical Technology — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Airway suction catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 724962a1-28a1-440f-b142-cf9118ade469 34 fields · synced Jun 7, 2026