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The Vest®System

FDA UDI

Class II (US FDA UDI)

by Hill-Rom Services Pte. Ltd.

Identity

Trade Name
The Vest®System FDA UDI
Generic Name
Chest-oscillation airway secretion-clearing system FDA UDI
Device Name
Contains 1 XS wrap, 1 S wrap, 2 L wrap, and 1 XL wrap. FDA UDI
Model / Reference
P300600005 FDA UDI
Description
Contains 1 XS wrap, 1 S wrap, 2 L wrap, and 1 XL wrap. FDA UDI

Identifiers

Primary DI / UDI-DI
00887761976849 FDA UDI
510(k) Number
K024309 FDA UDI
FDA Product Code
BYI FDA UDI
GMDN Term
Chest-oscillation airway secretion-clearing system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5665 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Category: Chest-oscillation airway secretion-clearing system

The Vest®System by Hill-Rom Services Pte. Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Chest-oscillation airway secretion-clearing system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hill-Rom Services Pte. Ltd.

Sources (1)

  • FDA UDI c17d3a36-ec53-4fc6-80f8-875006bf4eed 35 fields · synced May 29, 2026