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Straumann Surgical Cassettes

FDA UDI

Class II (US FDA UDI)

by Institut Straumann SA

Identity

Trade Name
Straumann Surgical Cassettes FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
Bone Block Fixation Cassette 1.5130 x 118 x 25 mm, thermoplast FDA UDI
Model / Reference
Storage Systems / Cassettes FDA UDI
Description
Bone Block Fixation Cassette 1.5130 x 118 x 25 mm, thermoplast FDA UDI

Identifiers

Catalog Number
041.032 FDA UDI
Primary DI / UDI-DI
07630031717917 FDA UDI
FDA Product Code
KCT FDA UDI
GMDN Term
Instrument tray, 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

Category: Instrument tray, reusable

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

Similar devices

Also classified as Instrument tray, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 70589b3f-0a96-4275-a937-cf0fedc222bd 35 fields · synced May 30, 2026