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Assy, Scan Board, Hill-Rom Progressa

FDA UDI

Class II (US FDA UDI)

by Neurologica Corporation

Identity

Trade Name
ASSY, SCAN BOARD, HILL-ROM PROGRESSA FDA UDI
Generic Name
Head/neck procedure positioner FDA UDI
Model / Reference
0-00139-001 FDA UDI

Identifiers

Primary DI / UDI-DI
10815411020144 FDA UDI
FDA Product Code
JAK FDA UDI
GMDN Term
Head/neck procedure positioner FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1750 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Head/neck procedure positioner

Assy, Scan Board, Hill-Rom Progressa by Neurologica Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Head/neck procedure positioner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8e3d77af-33d5-4b97-9e09-05367fff3b21 32 fields · synced May 31, 2026