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Reliance

FDA UDI

Class II (US FDA UDI)

by Corporation Steris Canada

Identity

Trade Name
Reliance FDA UDI
Generic Name
Endoscope drying/storage cabinet FDA UDI
Device Name
The 6000 Series Reliance Endoscope Drying and Storage Cabinet, 6 Scopes, Add-on (requires connectors) is designed to ensure a clean storage location for disinfected endoscopes and to protect the endoscopes from damage while in storage. FDA UDI
Model / Reference
6000 Series FDA UDI
Description
The 6000 Series Reliance Endoscope Drying and Storage Cabinet, 6 Scopes, Add-on (requires connectors) is designed to ensure a clean storage location for disinfected endoscopes and to protect the endoscopes from damage while in storage. FDA UDI

Identifiers

Catalog Number
REC6062DSA FDA UDI
Primary DI / UDI-DI
00724995179823 FDA UDI
FDA Product Code
PUP FDA UDI
GMDN Term
Endoscope drying/storage cabinet FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Endoscope drying/storage cabinet

Reliance by Corporation Steris Canada — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope drying/storage cabinet.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 36fbc341-8572-4c1c-894c-f9023fb2b354 35 fields · synced May 31, 2026