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Schwert

FDA UDI

Class I (US FDA UDI)

by A. Schweickhardt GmbH & Co. KG

Identity

Trade Name
SCHWERT FDA UDI
Generic Name
Periodontal curette FDA UDI
Device Name
Sickle scaler 204D for removing dental plaque from narrow interdental spaces in the premolar and frontal area 16,5cm FDA UDI
Model / Reference
3305-04SD FDA UDI
Description
Sickle scaler 204D for removing dental plaque from narrow interdental spaces in the premolar and frontal area 16,5cm FDA UDI

Identifiers

Catalog Number
3305-04SD FDA UDI
Primary DI / UDI-DI
E896330504SD0 FDA UDI
FDA Product Code
EMS FDA UDI
GMDN Term
Periodontal curette 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Periodontal curette

Schwert by A. Schweickhardt GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Periodontal curette.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a2f7aa5c-617b-4513-aa5c-f20c8f0ef438 35 fields · synced Jun 1, 2026