← Back to catalogue

Ferno2

FDA UDI

Class I (US FDA UDI)

by Spiracle Technology

Identity

Trade Name
FERNO2 FDA UDI
Generic Name
Emergency airway clearance suction system, manual FDA UDI
Device Name
MVP Manual Aspirator FDA UDI
Model / Reference
T60540 FDA UDI
Description
MVP Manual Aspirator FDA UDI

Identifiers

Primary DI / UDI-DI
00814940020048 FDA UDI
FDA Product Code
BSY FDA UDI
GMDN Term
Emergency airway clearance suction system, manual 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

No

FDA UDI

Single Use

No

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

Yes

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, manual

Ferno2 by Spiracle Technology — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Emergency airway clearance suction system, manual.

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
Spiracle Technology

Sources (1)

  • FDA UDI f433dedc-8d09-4d7c-b0c4-ab4819d9debb 33 fields · synced May 30, 2026