Identity
- Trade Name
- Rocket FDA UDI
- Generic Name
- Non-vascular catheter introduction set FDA UDI
- Device Name
- Rocket 26Fg Chest Catheter - Blunt Dissection Chest Drainage Insertion Pack FDA UDI
- Model / Reference
- R54549-26-PK FDA UDI
- Description
- Rocket 26Fg Chest Catheter - Blunt Dissection Chest Drainage Insertion Pack FDA UDI
Identifiers
- Catalog Number
- R54549-26-PK FDA UDI
- Primary DI / UDI-DI
- 05055270983237 FDA UDI
- FDA Product Code
- GBX FDA UDI
- GMDN Term
- Non-vascular catheter introduction set 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
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Non-vascular catheter introduction set
Rocket by Rocket Medical Plc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 |
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Manufacturer
- Manufacturer
- Rocket Medical Plc
Sources (1)
- FDA UDI 6c5b6d7c-3c46-4278-a47b-e835b636e2d8 34 fields · synced Jun 1, 2026