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Powerwand

FDA UDI

Class I (US FDA UDI)

by Access Scientific, Inc.

Identity

Trade Name
POWERWAND FDA UDI
Generic Name
Wearable percutaneous catheter/tube holder FDA UDI
Device Name
POWERWAND Dressing Change Kit with StatLock FDA UDI
Model / Reference
Dressing Change Kit with StatLock FDA UDI
Description
POWERWAND Dressing Change Kit with StatLock FDA UDI

Identifiers

Catalog Number
71697 FDA UDI
Primary DI / UDI-DI
10859821006374 FDA UDI
FDA Product Code
OXQ FDA UDI
GMDN Term
Wearable percutaneous catheter/tube holder FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5075 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Wearable percutaneous catheter/tube holder

Powerwand by Access Scientific, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wearable percutaneous catheter/tube holder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6ba743ef-d3b2-4f35-b153-4b99dca2d9ae 36 fields · synced Jun 6, 2026