devemed

FDA UDI

Class I (US FDA UDI)

by devemed GmbH

Identity

Trade Name: devemed FDA UDI
Generic Name: Dental suction system cannula, reusable FDA UDI
Device Name: dev-aspir 1 | Suction cannula tip Ø4.0mm Insert for # 2429-00 | with slot front: Ø 6.0/5.0mm; back: Ø 6.0/5.0mm FDA UDI
Model / Reference: 2429-30 FDA UDI
Description: dev-aspir 1 | Suction cannula tip Ø4.0mm Insert for # 2429-00 | with slot front: Ø 6.0/5.0mm; back: Ø 6.0/5.0mm FDA UDI

Identifiers

Primary DI / UDI-DI: 04061644032846 FDA UDI
FDA Product Code: KCB FDA UDI
GMDN Term: Dental suction system cannula, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 874.4420 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

Yes

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Serial Number

FDA UDI

Expiration Date

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Manufacturing Date

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Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Dental suction system cannula, reusable

devemed by devemed GmbH — 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: devemed GmbH

Sources (1)

FDA UDI 4688044c-66ad-4aa0-8480-94910990210b 34 fields · synced May 29, 2026