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Rocket

FDA UDI

by Rocket Medical Plc

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
MRI Safety
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

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Manufacturer

Manufacturer
Rocket Medical Plc

Sources (1)

  • FDA UDI 99c35078-32c0-404f-b747-b05f91db8793 37 fields · synced Jun 1, 2026