Sympress

FDA UDI

Class I (US FDA UDI)

by Renfert GmbH

Identity

Trade Name: SYMPRESS FDA UDI
Generic Name: Dental impression material mixer FDA UDI
Device Name: Dental impression material mixer, type 1 FDA UDI
Model / Reference: 60001000 FDA UDI
Description: Dental impression material mixer, type 1 FDA UDI

Identifiers

Catalog Number: 60001000 FDA UDI
Primary DI / UDI-DI: J009600010000 FDA UDI
FDA Product Code: EFD FDA UDI
GMDN Term: Dental impression material mixer FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.3100 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: Dental impression material mixer

Sympress by Renfert 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: Renfert GmbH

Sources (1)

FDA UDI 7a6ce431-3203-44ae-96ea-7cdf7a138fce 35 fields · synced Jun 8, 2026