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Marketlab, Inc

FDA UDI

Class I (US FDA UDI)

by Marketlab Inc.

Identity

Trade Name
Marketlab, Inc FDA UDI
Generic Name
Freestanding patient positioner, reusable FDA UDI
Device Name
Elevated Airway Positioner System, 3 pc. Complete Set (includes 1 Base, 1 Addition, 1 Headrest + 5 Covers) FDA UDI
Model / Reference
108198 FDA UDI
Description
Elevated Airway Positioner System, 3 pc. Complete Set (includes 1 Base, 1 Addition, 1 Headrest + 5 Covers) FDA UDI

Identifiers

Primary DI / UDI-DI
00817517026658 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Freestanding patient positioner, reusable

Marketlab, Inc by Marketlab 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

Manufacturer
Marketlab Inc.

Sources (1)

  • FDA UDI 03e9696e-113f-4a2c-a357-7e92c29ec00a 33 fields · synced May 31, 2026