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Trilogy

FDA UDI

Class II (US FDA UDI)

by Respironics, Inc.

Identity

Trade Name
Trilogy FDA UDI
Generic Name
Clinical laboratory information system FDA UDI
Device Name
RJ9 to 2.5mm 3" Female Adapter Cable FDA UDI
Model / Reference
RJ9 to 2.5mm 3" Female Adapter Cable FDA UDI
Description
RJ9 to 2.5mm 3" Female Adapter Cable FDA UDI

Identifiers

Catalog Number
1080250 FDA UDI
Primary DI / UDI-DI
00606959043244 FDA UDI
FDA Product Code
CBK FDA UDI
GMDN Term
Clinical laboratory information system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5895 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Clinical laboratory information system

Trilogy by Respironics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Clinical laboratory information system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Respironics, Inc.

Sources (1)

  • FDA UDI e22dffce-1002-4d62-86bc-c299ca5de9f0 36 fields · synced Jun 1, 2026