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Duck Bag

FDA UDI

Class I (US FDA UDI)

by Medisafe Uk Limited

Identity

Trade Name
Duck Bag FDA UDI
Generic Name
Medical device cleaning agent FDA UDI
Device Name
Duck Bag Full Din is a pre-moistened instrument bag, designed to maintain a safe and sealed humid environment for contaminated instruments during transportation between point of use and cleaning as an initial step of reprocessing. FDA UDI
Model / Reference
Duck Bag FDA UDI
Description
Duck Bag Full Din is a pre-moistened instrument bag, designed to maintain a safe and sealed humid environment for contaminated instruments during transportation between point of use and cleaning as an initial step of reprocessing. FDA UDI

Identifiers

Catalog Number
M20358 FDA UDI
Primary DI / UDI-DI
15060247263325 FDA UDI
FDA Product Code
NNK FDA UDI
GMDN Term
Medical device cleaning agent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3250 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Medical device cleaning agent

Duck Bag by Medisafe Uk Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical device cleaning agent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medisafe Uk Limited

Sources (1)

  • FDA UDI 1b40168a-8a44-48f8-ac76-ba847139a63b 35 fields · synced May 30, 2026