Identity
- Trade Name
- Rocket FDA UDI
- Generic Name
- Cerebrospinal fluid manometer, mechanical FDA UDI
- Device Name
- Spinal Manometer Set - EA FDA UDI
- Model / Reference
- R55990 FDA UDI
- Description
- Spinal Manometer Set - EA FDA UDI
Identifiers
- Catalog Number
- R55990 FDA UDI
- Primary DI / UDI-DI
- 05055270913395 FDA UDI
- GMDN Term
- Cerebrospinal fluid manometer, mechanical 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
No
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
Yes
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
Dimensions & Sizes
- Size
- Length — 40.0 Centimeter FDA UDI
Category: Cerebrospinal fluid manometer, mechanical
Rocket by Rocket Medical Plc — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Cerebrospinal fluid manometer, mechanical.
- Manometer Extension Tube - 20cm — Pajunk GmbH Medizintechnologie · Class II
- MANOMETER — Pajunk GmbH Medizintechnologie · Class II
- Spinal Manometer — Pajunk GmbH Medizintechnologie · 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 | N/A | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Rocket Medical Plc
Sources (1)
- FDA UDI 3a80739d-79f2-4dd8-adb4-68188670bbf2 37 fields · synced Jun 1, 2026