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SAVe1 Conversion Kit

FDA UDI

Class I (US FDA UDI)

by Safeguard Us Operating, Llc

Identity

Trade Name
SAVe1 Conversion Kit FDA UDI
Generic Name
Ventilator IMV supplemental circuit, single-use FDA UDI
Device Name
Automedx Conversion Kit FDA UDI
Model / Reference
02 FDA UDI
Description
Automedx Conversion Kit FDA UDI

Identifiers

Catalog Number
25-110-50 FDA UDI
Primary DI / UDI-DI
M6892511050020 FDA UDI
FDA Product Code
BZO FDA UDI
GMDN Term
Ventilator IMV supplemental circuit, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5975 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

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

No

FDA UDI

Category: Ventilator IMV supplemental circuit, single-use

SAVe1 Conversion Kit by Safeguard Us Operating, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ventilator IMV supplemental circuit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Safeguard Us Operating, Llc

Sources (1)

  • FDA UDI ee2d3b08-5ec0-4e61-94a7-525df7d9fb99 35 fields · synced May 30, 2026