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Rocket

FDA UDI

by Rocket Medical Plc

Identity

Trade Name
Rocket FDA UDI
Generic Name
Intrauterine curette, suction FDA UDI
Device Name
Rocket Swivel Handle 3/8" Soft Adaptor FDA UDI
Model / Reference
R57994 FDA UDI
Description
Rocket Swivel Handle 3/8" Soft Adaptor FDA UDI

Identifiers

Catalog Number
R57994 FDA UDI
Primary DI / UDI-DI
05055270915313 FDA UDI
GMDN Term
Intrauterine curette, suction 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
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Lumen/Inner Diameter — 15.85 Millimeter FDA UDI
Length — 2.0 Meter FDA UDI

Category: Intrauterine curette, suction

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

Similar devices

Also classified as Intrauterine curette, suction.

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 abcf0d77-e220-4794-b4eb-e085663cd217 37 fields · synced Jun 1, 2026