sentida 6 USA

FDA UDI

Class II (US FDA UDI)

by WISSNER-BOSSERHOFF GmbH

Identity

Trade Name: sentida 6 USA FDA UDI
Generic Name: Basic electric home bed FDA UDI
Device Name: Basic electric home bed FDA UDI
Model / Reference: 19-1077 FDA UDI
Description: Basic electric home bed FDA UDI

Identifiers

Primary DI / UDI-DI: 04050621100289 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 6 USA by WISSNER-BOSSERHOFF GmbH — 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: WISSNER-BOSSERHOFF GmbH

Sources (1)

FDA UDI a29778f3-a231-4965-8ec5-8e1703451819 33 fields · synced May 31, 2026