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Ferno #9 Conversion

FDA UDI

Class I (US FDA UDI)

by Lifeport, Llc.

Identity

Trade Name
Ferno #9 Conversion FDA UDI
Generic Name
Ambulance stretcher docking device FDA UDI
Device Name
TS-FERNO #9 CONVERSION ASSEMBLY * GRAY FDA UDI
Model / Reference
100-4206-02-05 FDA UDI
Description
TS-FERNO #9 CONVERSION ASSEMBLY * GRAY FDA UDI

Identifiers

Primary DI / UDI-DI
00810050863193 FDA UDI
FDA Product Code
FOX FDA UDI
GMDN Term
Ambulance stretcher docking device FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6990 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ambulance stretcher docking device

Ferno #9 Conversion by Lifeport, Llc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ambulance stretcher docking device.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Lifeport, Llc.

Sources (1)

  • FDA UDI 7b8c55d8-167c-4588-8570-839083b6c6d4 34 fields · synced Jun 6, 2026