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Integrity™

FDA UDI

Class II (US FDA UDI)

by Elekta Inc.

Identity

Trade Name
Integrity™ FDA UDI
Generic Name
Linear accelerator system FDA UDI
Device Name
Integrity FDA UDI
Model / Reference
1537146 FDA UDI
Description
Integrity FDA UDI

Identifiers

Primary DI / UDI-DI
05060191071345 FDA UDI
510(k) Number
K182138 FDA UDI
FDA Product Code
IYE FDA UDI
GMDN Term
Linear accelerator system 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

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

Category: Linear accelerator system

Integrity™ by Elekta Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Linear accelerator system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Elekta Inc.

Sources (1)

  • FDA UDI dd8a1492-6bfd-45b4-8c7c-6bd5b3c7ec84 35 fields · synced May 30, 2026