Identity
- Trade Name
- Rocket FDA UDI
- Generic Name
- Midstream urine specimen container IVD FDA UDI
- Device Name
- Rocket URIPOT Urine Specimen Pack FDA UDI
- Model / Reference
- R53084 FDA UDI
- Description
- Rocket URIPOT Urine Specimen Pack FDA UDI
Identifiers
- Catalog Number
- R53084 FDA UDI
- Primary DI / UDI-DI
- 05055270912589 FDA UDI
- GMDN Term
- Midstream urine specimen container IVD 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
Category: Midstream urine specimen container IVD
Rocket by Rocket Medical Plc — 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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Rocket Medical Plc
Sources (1)
- FDA UDI d17dbb8c-f5bd-4046-9ec4-b37bf43545e3 36 fields · synced May 30, 2026