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Mor-Medical New Era

FDA UDI

Class I (US FDA UDI)

by Moroles Investments, LLC

Identity

Trade Name
Mor-Medical New Era FDA UDI
Generic Name
Patient transfer sliding board FDA UDI
Device Name
Deluxe New Era Transfer Board, Half Size: 31" L x 23" W x 1/4" Thick FDA UDI
Model / Reference
DNE-TB-H FDA UDI
Description
Deluxe New Era Transfer Board, Half Size: 31" L x 23" W x 1/4" Thick FDA UDI

Identifiers

Primary DI / UDI-DI
00850010988795 FDA UDI
FDA Product Code
FMR FDA UDI
GMDN Term
Patient transfer sliding board FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6785 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: Patient transfer sliding board

Mor-Medical New Era by Moroles Investments, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient transfer sliding board.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6e01b1c6-520b-4104-b113-8ce8dd8fa6dd 33 fields · synced May 30, 2026