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Grid Panel

FDA UDI

Class II (US FDA UDI)

by Medtec LLC

Identity

Trade Name
Grid Panel FDA UDI
Generic Name
Indexed-immobilization patient positioning system FDA UDI
Device Name
Grid panel for Calypso 4D Localization System and Varian Exact base FDA UDI
Model / Reference
20IL430003 FDA UDI
Description
Grid panel for Calypso 4D Localization System and Varian Exact base FDA UDI

Identifiers

Catalog Number
20IL430003 FDA UDI
Primary DI / UDI-DI
00841439102053 FDA UDI
510(k) Number
K973842 FDA UDI
FDA Product Code
IXQ FDA UDI
GMDN Term
Indexed-immobilization patient positioning system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1980 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Width — 53 Centimeter FDA UDI
Length — 89.9 Centimeter FDA UDI

Grid Panel by Medtec LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K973842 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtec LLC

Sources (1)

  • FDA UDI cbfbfafa-6241-4750-9e42-806b17f64bcd 38 fields · synced Jun 1, 2026