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Prevalon

FDA UDI

Class I (US FDA UDI)

by Sage Products Llc

Identity

Trade Name
Prevalon FDA UDI
Generic Name
Patient transfer system, manual FDA UDI
Device Name
TrendeMATS Mobile Air Transfer System for Trendelenburg Position FDA UDI
Model / Reference
700-093 FDA UDI
Description
TrendeMATS Mobile Air Transfer System for Trendelenburg Position FDA UDI

Identifiers

Catalog Number
700-093 FDA UDI
Primary DI / UDI-DI
00618029980014 FDA UDI
FDA Product Code
FMR FDA UDI
KME FDA UDI
CCX FDA UDI
GMDN Term
Patient transfer system, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6785 FDA UDI
880.6060 FDA UDI
868.6820 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Convenience Kit

Yes

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
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Width — 39.0 Inch FDA UDI
Length — 81.0 Inch FDA UDI

Prevalon by Sage Products Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sage Products Llc

Sources (1)

  • FDA UDI ae0520ce-b860-49a7-a2de-693385d2669b 37 fields · synced May 30, 2026