sentida 03

FDA UDI

Class II (US FDA UDI)

by L I N E T spol. s r.o.

Identity

Trade Name: sentida 03 FDA UDI
Generic Name: Basic electric home bed FDA UDI
Device Name: Basic electric home bed FDA UDI
Model / Reference: 1WIS252739431011 FDA UDI
Description: Basic electric home bed FDA UDI

Identifiers

Primary DI / UDI-DI: 08592654186466 FDA UDI
FDA Product Code: LLI FDA UDI
GMDN Term: Basic electric home 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Basic electric home bed

sentida 03 by L I N E T spol. s r.o. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Long Term Care Bed — Dynarex Corp. · Class II
Footboard — Dynarex Corp. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: L I N E T spol. s r.o.

Sources (1)

FDA UDI e031e27e-5040-41ee-9a5a-4124df5cb649 33 fields · synced Jun 8, 2026