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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
Arm procedure positioner, reusable FDA UDI
Device Name
Arm Boards FDA UDI
Model / Reference
5200-3563 FDA UDI
Description
Arm Boards FDA UDI

Identifiers

Primary DI / UDI-DI
00850021301064 FDA UDI
FDA Product Code
NOD FDA UDI
GMDN Term
Arm procedure positioner, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.3910 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: Arm procedure 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 Arm procedure positioner, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 02c7b632-f38a-45bb-87f5-890760fa68e2 33 fields · synced May 30, 2026