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Large Manual Percussor Cup +1 more model

FDA UDI

Class I (US FDA UDI)

by Medicomp, Inc.

Identity

Trade Name
Large Manual Percussor Cup; 89mm FDA UDI
Generic Name
Manual chest percussor FDA UDI
Device Name
Large Manual Percussor Cup; 89mm FDA UDI
Model / Reference
MC-2289 FDA UDI
Description
Large Manual Percussor Cup; 89mm FDA UDI

Identifiers

Catalog Number
MC-2289 FDA UDI
Primary DI / UDI-DI
00858409005627 FDA UDI
FDA Product Code
GWZ FDA UDI
GMDN Term
Manual chest percussor FDA UDI
Models / Variants
Large Manual Percussor Cup FDA UDI
89mm FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
882.1700 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

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: Manual chest percussor

Large Manual Percussor Cup +1 more model by Medicomp, Inc. — Class I — FDA UDI — listed in FDA GUDID — 2 models — regulatory data on deviCERTS

Similar devices

Also classified as Manual chest percussor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medicomp, Inc.

Sources (1)

  • FDA UDI 3697b769-5559-4e0a-b0a5-95409e8fabb8 34 fields · synced May 30, 2026