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Guide Pins

FDA UDI

Class II (US FDA UDI)

by Medtec LLC

Identity

Trade Name
Guide Pins FDA UDI
Generic Name
Radiological general body-part positioner FDA UDI
Device Name
For use with Varian Exact™ Couchtop FDA UDI
Model / Reference
109013 FDA UDI
Description
For use with Varian Exact™ Couchtop FDA UDI

Identifiers

Catalog Number
109013 FDA UDI
Primary DI / UDI-DI
00841439100462 FDA UDI
510(k) Number
K060737 FDA UDI
FDA Product Code
IYE FDA UDI
GMDN Term
Radiological general body-part positioner FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.5050 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 2.5 Centimeter FDA UDI
Outer Diameter — 2.4 Centimeter FDA UDI

Guide Pins by Medtec LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtec LLC

Sources (1)

  • FDA UDI e226ee76-2098-4f7e-b955-a66d1557f560 38 fields · synced May 31, 2026