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Dry320

FDA UDI

Class I (US FDA UDI)

by Wassenburg Medical, Inc.

Identity

Trade Name
DRY320 FDA UDI
Generic Name
Endoscope drying/storage cabinet FDA UDI
Device Name
A device to store and dry endoscopes FDA UDI
Model / Reference
DRY320 FDA UDI
Description
A device to store and dry endoscopes FDA UDI

Identifiers

Primary DI / UDI-DI
DRY320 FDA UDI
FDA Product Code
JRJ FDA UDI
GMDN Term
Endoscope drying/storage cabinet FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Dry320 by Wassenburg Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ad376e23-da78-42c2-9a19-7253bcb6caa8 35 fields · synced Jun 1, 2026