← Back to catalogue

C-Arm Solid Panel Insert

FDA UDI

Class II (US FDA UDI)

by Aktina Corp.

Identity

Trade Name
C-Arm Solid Panel Insert FDA UDI
Generic Name
Radiological whole-body positioner FDA UDI
Model / Reference
11-211 FDA UDI

Identifiers

Primary DI / UDI-DI
B365112110 FDA UDI
510(k) Number
K032248 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Radiological whole-body positioner

C-Arm Solid Panel Insert by Aktina Corp. — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Aktina Corp.

Sources (1)

  • FDA UDI b3a8eec3-d15b-4471-a41f-b4ff3656699b 33 fields · synced Jun 7, 2026