Excom hybrid

FDA UDI

Class I (US FDA UDI)

by Ritter Concept GmbH

Identity

Trade Name: Excom hybrid FDA UDI
Generic Name: Dental suction system FDA UDI
Model / Reference: Excom hybrid 5 FDA UDI

Identifiers

Primary DI / UDI-DI: ERICEH500000 FDA UDI
FDA Product Code: EBR FDA UDI
GMDN Term: Dental suction system FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.6640 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

MRI Safety

MR Unsafe FDA UDI

Category: Dental suction system

Excom hybrid by Ritter Concept 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: Ritter Concept GmbH

Sources (1)

FDA UDI 7344f087-178a-4141-8a98-805d051ea39b 33 fields · synced May 30, 2026