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CAS-One IR

FDA UDI

Class II (US FDA UDI)

by CAScination AG

Identity

Trade Name
CAS-One IR FDA UDI
Generic Name
Multi-purpose stereotactic surgery system FDA UDI
Model / Reference
2.0 FDA UDI

Identifiers

Primary DI / UDI-DI
07640167222131 FDA UDI
510(k) Number
K152473 FDA UDI
FDA Product Code
JAK FDA UDI
GMDN Term
Multi-purpose stereotactic surgery system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1750 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Multi-purpose stereotactic surgery system

CAS-One IR by CAScination AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-purpose stereotactic surgery system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
CAScination AG

Sources (1)

  • FDA UDI 9403d410-0848-46b4-b5f9-549c60b2fb8b 33 fields · synced May 30, 2026