Identity
- Trade Name
- Rocket FDA UDI
- Generic Name
- Intrauterine imaging medium catheter FDA UDI
- Device Name
- Rocket Cervix Adaptor Large - 30mm FDA UDI
- Model / Reference
- R57491 FDA UDI
- Description
- Rocket Cervix Adaptor Large - 30mm FDA UDI
Identifiers
- Catalog Number
- R57491 FDA UDI
- Primary DI / UDI-DI
- 05055270900357 FDA UDI
- GMDN Term
- Intrauterine imaging medium catheter 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
- Outer Diameter — 30.0 Millimeter FDA UDI
Category: Intrauterine imaging medium catheter
Rocket by Rocket Medical Plc — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Intrauterine imaging medium catheter.
- Cook — COOK INCORPORATED · Class II
- uVue — COOK INCORPORATED · Class II
- Batrik H/S Catheter TM 5F — Batrik Medical Manufacturing Inc · Class II
- Cook — COOK INCORPORATED · Class I
- Mencini — COOK INCORPORATED · Class II
- Tenacath — COOK INCORPORATED · Class II
- Cook — COOK INCORPORATED · Class II
- Hysterosalpingography (HSG) Catheter — Argon Medical Devices, Inc. · 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 |
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Manufacturer
- Manufacturer
- Rocket Medical Plc
Sources (1)
- FDA UDI c849ccc1-cda4-4242-ae05-a7123a017146 37 fields · synced Jun 8, 2026