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Straumann BLX Surgical Cassette

FDA UDI

Class II (US FDA UDI)

by Institut Straumann SA

Identity

Trade Name
Straumann BLX Surgical Cassette FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
BLX Surgical cassette FDA UDI
Model / Reference
Storage Systems / Cassettes FDA UDI
Description
BLX Surgical cassette FDA UDI

Identifiers

Catalog Number
069.0001 FDA UDI
Primary DI / UDI-DI
07630031744791 FDA UDI
510(k) Number
K180791 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Instrument tray, reusable

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

Similar devices

Also classified as Instrument tray, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2b9d9090-bc09-4317-a424-92e06b4df061 36 fields · synced Jun 6, 2026