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Posirest 2

FDA UDI

Class II (US FDA UDI)

by Medtec LLC

Identity

Trade Name
Posirest 2 FDA UDI
Generic Name
Radiological breast positioner, non-wearable FDA UDI
Device Name
Baseplate with headrest, high arm support, cranial arm support and adjustable arm supports (2) FDA UDI
Model / Reference
106520 FDA UDI
Description
Baseplate with headrest, high arm support, cranial arm support and adjustable arm supports (2) FDA UDI

Identifiers

Catalog Number
106520 FDA UDI
Primary DI / UDI-DI
00841439100332 FDA UDI
510(k) Number
K060737 FDA UDI
FDA Product Code
IYE FDA UDI
GMDN Term
Radiological breast positioner, non-wearable 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

Yes

FDA UDI

Dimensions & Sizes

Size
Width — 17.8 Inch FDA UDI
Length — 25.3 Inch FDA UDI

Category: Radiological breast positioner, non-wearable

Posirest 2 by Medtec LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiological breast positioner, non-wearable.

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 13e0b4e7-c706-459e-9e03-a7891b8e17c6 37 fields · synced May 30, 2026