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Straumann Modular Cassette

FDA UDI

Class II (US FDA UDI)

by Institut Straumann SA

Identity

Trade Name
Straumann Modular Cassette FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Device Name
A Module, Release Aid Tray FDA UDI
Model / Reference
Storage Systems / Cassettes FDA UDI
Description
A Module, Release Aid Tray FDA UDI

Identifiers

Catalog Number
041.767 FDA UDI
Primary DI / UDI-DI
07630031740007 FDA UDI
FDA Product Code
KCT FDA UDI
GMDN Term
Device sterilization/disinfection container, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6850 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Device sterilization/disinfection container, reusable

Straumann Modular Cassette by Institut Straumann SA — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 41ffd6ae-d86d-4ec0-b8e5-27a0085c8bf6 35 fields · synced Jun 1, 2026