Identity
- Trade Name
- Heimlich valve FDA UDI
- Generic Name
- Pleural drainage valve FDA UDI
- Device Name
- The Heimlich non-return valve is a one-way drainage device which prevents the air reflux towards the patient's chest. FDA UDI
- Model / Reference
- 10530 FDA UDI
- Description
- The Heimlich non-return valve is a one-way drainage device which prevents the air reflux towards the patient's chest. FDA UDI
Identifiers
- Catalog Number
- 10530 FDA UDI
- Primary DI / UDI-DI
- 08034139291130 FDA UDI
- FDA Product Code
- KDQ FDA UDI
- GMDN Term
- Pleural drainage valve FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Pleural drainage valve
Heimlich valve by Redax Spa — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Pleural drainage valve.
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- CMC MED SOLUTIONS — CMC Manufacturing Limited Liability Company · Class II
- CMC MED SOLUTIONS — CMC Manufacturing Limited Liability Company · Class II
- Synchronis — SYNCHRONIS MEDICAL LLC · Class II
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 II | Pending data |
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Manufacturer
- Manufacturer
- Redax Spa
Sources (1)
- FDA UDI dcd45105-c159-4137-8f56-dda2e5bd6ff1 36 fields · synced May 30, 2026