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Amsco

FDA UDI

Class II (US FDA UDI)

by Corporation Steris Canada

Identity

Trade Name
AMSCO FDA UDI
Generic Name
Endoscope drying/storage cabinet FDA UDI
Device Name
The AMSCO Drying Cabinet, 29-inch with Pass Through delivers unrivaled precision with exact temperature control, timers for every shelf and HEPA filtration. FDA UDI
Model / Reference
Drying Cabinet FDA UDI
Description
The AMSCO Drying Cabinet, 29-inch with Pass Through delivers unrivaled precision with exact temperature control, timers for every shelf and HEPA filtration. FDA UDI

Identifiers

Catalog Number
DCR100101 FDA UDI
Primary DI / UDI-DI
00724995162610 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

Amsco 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 5ddeb3ea-595b-4d7d-ad8d-3fa1e9a6832c 35 fields · synced May 31, 2026