← Back to catalogue

PowerGlide Midline Catheter

FDA UDI

Class II (US FDA UDI)

by Bard Access Systems, Inc.

Identity

Trade Name
PowerGlide Midline Catheter FDA UDI
Generic Name
Peripheral vascular catheter FDA UDI
Device Name
PowerGlide 20G 8cm Basic FDA UDI
Model / Reference
M120080 FDA UDI
Description
PowerGlide 20G 8cm Basic FDA UDI

Identifiers

Catalog Number
M120080 FDA UDI
Primary DI / UDI-DI
00801741075315 FDA UDI
FDA Product Code
FOZ FDA UDI
GMDN Term
Peripheral vascular 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

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

Dimensions & Sizes

Size
Length — 8 Centimeter FDA UDI

Category: Peripheral vascular catheter

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

Similar devices

Also classified as Peripheral vascular catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 4f6d3cde-988a-4276-860e-b56dc5c9b2de 36 fields · synced Jun 9, 2026