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Pinestar Technology Inc

FDA UDI

Class I (US FDA UDI)

by Pinestar Technology Inc.

Identity

Trade Name
Pinestar Technology Inc FDA UDI
Generic Name
Freestanding patient positioner, reusable FDA UDI
Device Name
Prone Breast Imaging Separation Pad FDA UDI
Model / Reference
PBI-L FDA UDI
Description
Prone Breast Imaging Separation Pad FDA UDI

Identifiers

Primary DI / UDI-DI
00850021301385 FDA UDI
FDA Product Code
CCX FDA UDI
GMDN Term
Freestanding patient positioner, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6820 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Freestanding patient positioner, reusable

Pinestar Technology Inc by Pinestar Technology Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Freestanding patient positioner, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a3e2aae7-dc11-477f-9b59-3214fa457f1a 33 fields · synced May 30, 2026