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iCAST H&S Micro 2mm

FDA UDI

Class II (US FDA UDI)

by IT-V Medizintechnik GmbH

Identity

Trade Name
iCAST H&S Micro 2mm FDA UDI
Generic Name
Radiological whole-body positioner FDA UDI
Model / Reference
P10107-305 FDA UDI

Identifiers

Primary DI / UDI-DI
09120074393059 FDA UDI
510(k) Number
K081218 FDA UDI
FDA Product Code
IYE FDA UDI
GMDN Term
Radiological whole-body positioner FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.5050 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

No

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Radiological whole-body positioner

iCAST H&S Micro 2mm by IT-V Medizintechnik GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiological whole-body positioner.

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 d5e8e041-7a98-49e0-8091-a2d5253aca6a 33 fields · synced May 30, 2026