← Back to catalogue

DeRoyal

FDA UDI

Class II (US FDA UDI)

by Deroyal Industries, Inc.

Identity

Trade Name
DeRoyal FDA UDI
Generic Name
Surgical suction system collection container, reusable FDA UDI
Device Name
DRAIN JUG FDA UDI
Model / Reference
30-6008 FDA UDI
Description
DRAIN JUG FDA UDI

Identifiers

Catalog Number
30-6008 FDA UDI
Primary DI / UDI-DI
00749756733052 FDA UDI
FDA Product Code
KDQ FDA UDI
GMDN Term
Surgical suction system collection container, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical suction system collection container, reusable

DeRoyal by Deroyal Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical suction system collection container, reusable.

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

Sources (1)

  • FDA UDI c826d75e-7790-4444-a884-e4c4dbc4cfaf 35 fields · synced Jun 8, 2026