Rocket

FDA UDI

by Rocket Medical Plc

Identity

Trade Name: Rocket FDA UDI
Generic Name: Pneumothorax catheter insertion set FDA UDI
Device Name: Rocket 24Fg Seldinger Chest Drainage Kit FDA UDI
Model / Reference: R51549-24-PK FDA UDI
Description: Rocket 24Fg Seldinger Chest Drainage Kit FDA UDI

Identifiers

Catalog Number: R51549-24-PK FDA UDI
Primary DI / UDI-DI: 05055270973450 FDA UDI
GMDN Term: Pneumothorax catheter insertion set FDA UDI

Classification

Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

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

Dimensions & Sizes

Size: Length — 40.0 Centimeter FDA UDI
Catheter Gauge — 24.0 French FDA UDI

Category: Pneumothorax catheter insertion set

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

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Also classified as Pneumothorax catheter insertion set.

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ARROW — TELEFLEX INCORPORATED · Class II
TMM-CT-SO (Tactical Medical Module-Chest Tube-Special Operations) — Altitude Technologies Inc. · Class I
ARROW — TELEFLEX INCORPORATED · Class II
Thora-Vent Thoracic Vent — Uresil Corp. · Class II
ARROW — TELEFLEX INCORPORATED · Class II
H&H Chest Tube Insertion Kit — H & H Medical Corporation

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 56b764e5-6a5e-4058-b889-457ac5a5899d 37 fields · synced Jun 8, 2026