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Venti-Scan Iv

FDA UDI

Class II (US FDA UDI)

by Biodex Medical Systems

Identity

Trade Name
VENTI-SCAN IV FDA UDI
Generic Name
Radioaerosol administration set FDA UDI
Device Name
KIT, CONVENIENCE, VENTI-PAK FOR VENTI SCAN (ADAPTER KIT FOR VENTILATOR ASSISTED PATIENTS FDA UDI
Model / Reference
177-075 FDA UDI
Description
KIT, CONVENIENCE, VENTI-PAK FOR VENTI SCAN (ADAPTER KIT FOR VENTILATOR ASSISTED PATIENTS FDA UDI

Identifiers

Catalog Number
177-075 FDA UDI
Primary DI / UDI-DI
00718175005156 FDA UDI
510(k) Number
K871868 FDA UDI
FDA Product Code
IYT FDA UDI
GMDN Term
Radioaerosol administration set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1390 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Radioaerosol administration set

Venti-Scan Iv by Biodex Medical Systems — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radioaerosol administration set.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 50dbfc34-d7b9-4dee-bc9e-0638d07d9df7 35 fields · synced May 30, 2026