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Rocket

FDA UDI

Class I (US FDA UDI)

by Rocket Medical Plc

Identity

Trade Name
Rocket FDA UDI
Generic Name
Surgical suction system collection container, single-use FDA UDI
Device Name
Single Chamber Chest Drainage Bottle with Droplet Control Shroud & Tubing Set FDA UDI
Model / Reference
R54517 FDA UDI
Description
Single Chamber Chest Drainage Bottle with Droplet Control Shroud & Tubing Set FDA UDI

Identifiers

Catalog Number
R54517 FDA UDI
Primary DI / UDI-DI
05055270975614 FDA UDI
FDA Product Code
GCY FDA UDI
GMDN Term
Surgical suction system collection container, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4680 FDA UDI
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

No

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical suction system collection container, single-use

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

Similar devices

Also classified as Surgical suction system collection container, single-use.

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 ec6a4b4b-bfd1-4af1-ad92-fff04829230f 34 fields · synced May 30, 2026