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DeRoyal

FDA UDI

Class II (US FDA UDI)

by Pergo Medikal Ve Ilac Sanayi Anonim Sirketi

Identity

Trade Name
DeRoyal FDA UDI
Generic Name
Suction system canister liner FDA UDI
Device Name
Suction Liner HF 3000 ml (Sample Port, Individual Pack) FDA UDI
Model / Reference
71-BG3000-PE FDA UDI
Description
Suction Liner HF 3000 ml (Sample Port, Individual Pack) FDA UDI

Identifiers

Primary DI / UDI-DI
08682952419431 FDA UDI
FDA Product Code
GCX FDA UDI
GMDN Term
Suction system canister liner 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

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 canister liner

DeRoyal by Pergo Medikal Ve Ilac Sanayi Anonim Sirketi — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suction system canister liner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b526340b-6c03-437d-90f9-8b758d3c55b6 33 fields · synced May 30, 2026