VivaSight DL AS Set Includes

FDA UDI

Class II (US FDA UDI)

by Etview , Ltd.

Identity

Trade Name: VivaSight DL AS Set Includes FDA UDI
Generic Name: Endobronchial tube FDA UDI
Device Name: Visualized double lumen endobronchial tube set. The set includes DLVT41 tube + adapter cable, two suction catheter 8RF and two mully suction catheter 10RF+Finger tip. FDA UDI
Model / Reference: DLVT41LAS FDA UDI
Description: Visualized double lumen endobronchial tube set. The set includes DLVT41 tube + adapter cable, two suction catheter 8RF and two mully suction catheter 10RF+Finger tip. FDA UDI

Identifiers

Catalog Number: DLVT41LAS FDA UDI
Primary DI / UDI-DI: 07290013745736 FDA UDI
510(k) Number: K123853 FDA UDI
FDA Product Code: CBI FDA UDI
GMDN Term: Endobronchial tube FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5740 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Ethylene Oxide FDA UDI

Category: Endobronchial tube

VivaSight DL AS Set Includes by Etview , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Endobronchial tube.

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Endobronchial Tube — Well Lead Medical Co., Ltd · Class II

Cleared under the same submission

K123853 also covers:

VivaSight DL AS Set Includes — Etview , Ltd.
VivaSight DL AS Set Includes — Etview , Ltd.
VivaSight DL AS Set Includes — Etview , Ltd.
VivaSight-DL — Etview , Ltd.
VivaSight-DL — Etview , Ltd.
VivaSight-DL — Etview , Ltd.
VivaSight-DL — Etview , Ltd.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Etview , Ltd.

Sources (1)

FDA UDI d35bbcc6-f939-43dc-a827-fdbaa836ebf3 36 fields · synced May 31, 2026