Identity
- Trade Name
- Rocket FDA UDI
- Generic Name
- Closed-wound drainage kit, micro-drainage FDA UDI
- Device Name
- Rocket KCH Fetal Bladder Catheter FDA UDI
- Model / Reference
- R57405 FDA UDI
- Description
- Rocket KCH Fetal Bladder Catheter FDA UDI
Identifiers
- Catalog Number
- R57405 FDA UDI
- Primary DI / UDI-DI
- 05055270913678 FDA UDI
- PMA Number
- H970001 FDA UDI
- GMDN Term
- Closed-wound drainage kit, micro-drainage FDA UDI
Classification
- 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
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
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Safe FDA UDI
Category: Closed-wound drainage kit, micro-drainage
Rocket by Rocket Medical Plc — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Closed-wound drainage kit, micro-drainage.
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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Rocket Medical Plc
Sources (1)
- FDA UDI 99c35078-32c0-404f-b747-b05f91db8793 37 fields · synced Jun 1, 2026