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Titan

FDA UDI

Class II (US FDA UDI)

by Nu Dimension Tech Ventures LLC

Identity

Trade Name
TITAN FDA UDI
Generic Name
Stand-up bed FDA UDI
Device Name
Electrical bed for healthcare, 36x84 inch FDA UDI
Model / Reference
LB600 FDA UDI
Description
Electrical bed for healthcare, 36x84 inch FDA UDI

Identifiers

Primary DI / UDI-DI
TITANLB600 FDA UDI
FDA Product Code
FNL FDA UDI
GMDN Term
Stand-up bed FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5100 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

Yes

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: Stand-up bed

Titan by Nu Dimension Tech Ventures LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stand-up bed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0f008db5-64e2-407e-bd7b-5db8bcb48ce9 33 fields · synced May 30, 2026