Acemst1

FDA UDI

Class I (US FDA UDI)

by Acem Spa

Identity

Trade Name: ACEMST1 FDA UDI
Generic Name: Fixed examination/treatment room light FDA UDI
Device Name: ACEMST1.3 FLEXIBLE ARM WALL FDA UDI
Model / Reference: ACEMST1.3 /FW FDA UDI
Description: ACEMST1.3 FLEXIBLE ARM WALL FDA UDI

Identifiers

Catalog Number: 111102 FDA UDI
Primary DI / UDI-DI: 08050705890231 FDA UDI
FDA Product Code: KZF FDA UDI
GMDN Term: Fixed examination/treatment room light FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.6320 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

Yes

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: Fixed examination/treatment room light

Acemst1 by Acem Spa — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 I	Pending data

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Manufacturer

Manufacturer: Acem Spa

Sources (1)

FDA UDI ac41ed14-233b-4e94-b90d-d0d7b7f5b215 34 fields · synced Jun 8, 2026