Reicodent

FDA UDI

Class I (US FDA UDI)

by devemed GmbH

Identity

Trade Name: Reicodent FDA UDI
Generic Name: Periodontal file/rasp, manual FDA UDI
Device Name: Periodontal file # 3S-4S "Sugarman"; Buccal / Lingual COMFORT | SL | double ended FDA UDI
Model / Reference: 02-SU 3-4 C FDA UDI
Description: Periodontal file # 3S-4S "Sugarman"; Buccal / Lingual COMFORT | SL | double ended FDA UDI

Identifiers

Primary DI / UDI-DI: 04061644036639 FDA UDI
FDA Product Code: EMR FDA UDI
GMDN Term: Periodontal file/rasp, manual FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.4565 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

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Periodontal file/rasp, manual

Reicodent 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 3ab0f2b5-07aa-42f0-b60a-ad78b20d04f2 34 fields · synced May 31, 2026