Identity
- Trade Name
- MedDrain FDA UDI
- Generic Name
- Pleural catheter FDA UDI
- Device Name
- MedDrain 28 Fr Right Angle Thoracic Catheter 6 Eyes, Coated FDA UDI
- Model / Reference
- 232028C FDA UDI
- Description
- MedDrain 28 Fr Right Angle Thoracic Catheter 6 Eyes, Coated FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10850082007636 FDA UDI
- FDA Product Code
- KGZ FDA UDI
- GMDN Term
- Pleural catheter FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4200 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 catheter
MedDrain by Armm Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Pleural catheter.
- Axiom® Atraum™ With ClotStop® — AXIOM MEDICAL, INCORPORATED · Class I
- Axiom® PVC — AXIOM MEDICAL, INCORPORATED · Class I
- Wayne — COOK INCORPORATED · Class II
- Axiom® PVC — AXIOM MEDICAL, INCORPORATED · Class I
- Axiom® PVC — AXIOM MEDICAL, INCORPORATED · Class I
- PLEUR-EVAC — TELEFLEX INCORPORATED · Class I
- Rocket — Rocket Medical Plc · Class I
- Axiom® — AXIOM MEDICAL, INCORPORATED · 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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Armm Inc.
Sources (1)
- FDA UDI c0c49778-0f35-40f8-a6d4-7900a5beee79 34 fields · synced May 30, 2026