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Brachial Plexus SatPad™

FDA UDI

Class II (US FDA UDI)

by Sat Pad Inc.

Identity

Trade Name
Brachial Plexus SatPad™ FDA UDI
Generic Name
Radiological headrest FDA UDI
Device Name
Brachial Plexus Radiological positioning devise for MR FDA UDI
Model / Reference
1 FDA UDI
Description
Brachial Plexus Radiological positioning devise for MR FDA UDI

Identifiers

Catalog Number
100010 FDA UDI
Primary DI / UDI-DI
00850004813102 FDA UDI
510(k) Number
K926416 FDA UDI
FDA Product Code
LNH FDA UDI
GMDN Term
Radiological headrest FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1000 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

No

FDA UDI

Category: Radiological headrest

Brachial Plexus SatPad™ by Sat Pad Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiological headrest.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sat Pad Inc.

Sources (1)

  • FDA UDI d4307b6d-857d-43c5-a161-b3377cb9974e 36 fields · synced May 30, 2026