Identity
- Trade Name
- Pediatric Manual Percussor Cup FDA UDI
- Generic Name
- Manual chest percussor FDA UDI
- Device Name
- Pediatric Manual Percussor Cup; 47mm FDA UDI
- Model / Reference
- MC-2247 FDA UDI
- Description
- Pediatric Manual Percussor Cup; 47mm FDA UDI
Identifiers
- Catalog Number
- MC-2247 FDA UDI
- Primary DI / UDI-DI
- 00858409005313 FDA UDI
- FDA Product Code
- GWZ FDA UDI
- GMDN Term
- Manual chest percussor 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
Pediatric Manual Percussor Cup by Medicomp, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Manual chest percussor.
- Portex — ICU MEDICAL, INC. · Class II
- Portex — ICU MEDICAL, INC. · Class II
- Portex — ICU MEDICAL, INC. · Class II
- Portex — ICU MEDICAL, INC. · Class II
- Medium Manual Percussor Cup — MEDICOMP, INC. · Class I
- Large Manual Percussor Cup; 89mm — MEDICOMP, INC. · Class I
- Neonatal Manual Percussor Cup — MEDICOMP, INC. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Medicomp, Inc.
Sources (1)
- FDA UDI cb3ea53b-641e-493e-af47-245c9dbdcc91 34 fields · synced May 30, 2026