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Rocket

FDA UDI

by Rocket Medical Plc

Identity

Trade Name
Rocket FDA UDI
Generic Name
Assisted reproduction catheter set FDA UDI
Device Name
Rocket DUO IUI Catheter 23cm FDA UDI
Model / Reference
R57625-00-23 FDA UDI
Description
Rocket DUO IUI Catheter 23cm FDA UDI

Identifiers

Catalog Number
R57625-00-23 FDA UDI
Primary DI / UDI-DI
05055270914514 FDA UDI
510(k) Number
K980061 FDA UDI
GMDN Term
Assisted reproduction catheter set 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

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

Dimensions & Sizes

Size
Length — 23.0 Centimeter FDA UDI

Category: Assisted reproduction catheter set

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

Similar devices

Also classified as Assisted reproduction catheter set.

Cleared under the same submission

K980061 also covers:

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 a949e0ed-4ca1-4189-9ff8-79b1154b228d 38 fields · synced May 30, 2026