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PowerGlide

FDA UDI

Class II (US FDA UDI)

by Bard Access Systems, Inc.

Identity

Trade Name
PowerGlide FDA UDI
Generic Name
Peripheral vascular intervention infusion catheter FDA UDI
Device Name
PowerGlide Pro with Reinforced Tip, 20G 10cm, Full Kit FDA UDI
Model / Reference
F120101T FDA UDI
Description
PowerGlide Pro with Reinforced Tip, 20G 10cm, Full Kit FDA UDI

Identifiers

Catalog Number
F120101T FDA UDI
Primary DI / UDI-DI
00801741142727 FDA UDI
FDA Product Code
FOZ FDA UDI
GMDN Term
Peripheral vascular intervention infusion catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5200 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

Yes

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

Dimensions & Sizes

Size
Length — 10 Centimeter FDA UDI

Category: Peripheral vascular intervention infusion catheter

PowerGlide by Bard Access Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral vascular intervention infusion catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bard Access Systems, Inc.

Sources (1)

  • FDA UDI 98d67c62-48a5-4d47-8183-51bf3deccfe1 37 fields · synced Jun 9, 2026