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Sterilization Tray Cirq® Robotic Alignment LITT

FDA UDI

Class II (US FDA UDI)

by Brainlab SE

Identity

Trade Name
Sterilization Tray Cirq® Robotic Alignment LITT FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Model / Reference
52337A FDA UDI

Identifiers

Primary DI / UDI-DI
04056481146719 FDA UDI
510(k) Number
K243698 FDA UDI
FDA Product Code
HAW FDA UDI
GMDN Term
Device sterilization/disinfection container, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4560 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Device sterilization/disinfection container, reusable

Sterilization Tray Cirq® Robotic Alignment LITT by Brainlab SE — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Brainlab SE

Sources (1)

  • FDA UDI eac8ea1e-d630-469f-af9d-47e33062653b 33 fields · synced May 30, 2026