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V7

FDA UDI

Class II (US FDA UDI)

by Hersill Sl

Identity

Trade Name
V7 FDA UDI
Generic Name
Emergency airway clearance suction system, electric FDA UDI
Device Name
V7 G emergency suction unit FDA UDI
Model / Reference
V7 G FDA UDI
Description
V7 G emergency suction unit FDA UDI

Identifiers

Catalog Number
5320220 FDA UDI
Primary DI / UDI-DI
08435331770575 FDA UDI
510(k) Number
K093241 FDA UDI
FDA Product Code
BTA FDA UDI
GMDN Term
Emergency airway clearance suction system, electric FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4780 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Emergency airway clearance suction system, electric

V7 by Hersill Sl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Emergency airway clearance suction system, electric.

Cleared under the same submission

K093241 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hersill Sl

Sources (1)

  • FDA UDI 7f3ddef6-2c72-4930-b5ba-d055403d7387 35 fields · synced May 30, 2026