← Back to catalogue

Rocket

FDA UDI

Class I (US FDA UDI)

by Rocket Medical Plc

Identity

Trade Name
Rocket FDA UDI
Generic Name
Suction system filter, microbial FDA UDI
Device Name
Water Trap Set for CRAFT™ Suction Pumps FDA UDI
Model / Reference
R57685 FDA UDI
Description
Water Trap Set for CRAFT™ Suction Pumps FDA UDI

Identifiers

Catalog Number
R57685 FDA UDI
Primary DI / UDI-DI
05055270986504 FDA UDI
FDA Product Code
NVT FDA UDI
GMDN Term
Suction system filter, microbial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.1700 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: Suction system filter, microbial

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

Similar devices

Also classified as Suction system filter, microbial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Rocket Medical Plc

Sources (1)

  • FDA UDI eb312f6e-f977-44bb-903a-1fcee06494ab 34 fields · synced Jun 8, 2026