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Rocket

FDA UDI

Class II (US FDA UDI)

by Rocket Medical Plc

Identity

Trade Name
Rocket FDA UDI
Generic Name
Surgical suction pump FDA UDI
Device Name
CRAFT™ Suction Pump (110V) FDA UDI
Model / Reference
R29654 FDA UDI
Description
CRAFT™ Suction Pump (110V) FDA UDI

Identifiers

Catalog Number
R29654 FDA UDI
Primary DI / UDI-DI
05055270911575 FDA UDI
FDA Product Code
GCX FDA UDI
GMDN Term
Surgical suction pump FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical suction pump

Rocket by Rocket Medical Plc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical suction pump.

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 7d887283-4a5c-4b11-9f53-84c12e24f916 34 fields · synced May 29, 2026