← Back to catalogue

VivaSight-DL

FDA UDI

Class II (US FDA UDI)

by Etview , Ltd.

Identity

Trade Name
VivaSight-DL FDA UDI
Generic Name
Endobronchial tube FDA UDI
Device Name
Visualized double lumen endobronchial tube set. The set contains 1 DL tube, two pouches of suction catheter straight and two pouches of suction catheter curved. FDA UDI
Model / Reference
DLVT37 FDA UDI
Description
Visualized double lumen endobronchial tube set. The set contains 1 DL tube, two pouches of suction catheter straight and two pouches of suction catheter curved. FDA UDI

Identifiers

Catalog Number
DLVT37 FDA UDI
Primary DI / UDI-DI
07290013745606 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

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Endobronchial tube

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

Similar devices

Also classified as Endobronchial tube.

Cleared under the same submission

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
Etview , Ltd.

Sources (1)

  • FDA UDI 8d8fe4e1-f8e6-4560-a098-f07708511c4b 36 fields · synced Jun 6, 2026