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Vascband

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
VASCBAND FDA UDI
Generic Name
Radial artery compression device FDA UDI
Device Name
VascBand Inflation Syringe 29cm Ex Long FDA UDI
Model / Reference
IPN914176 FDA UDI
Description
VascBand Inflation Syringe 29cm Ex Long FDA UDI

Identifiers

Catalog Number
3529 FDA UDI
Primary DI / UDI-DI
10841156102067 FDA UDI
FDA Product Code
DXC FDA UDI
GMDN Term
Radial artery compression device FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4450 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 — 29 Centimeter FDA UDI

Category: Radial artery compression device

Vascband by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radial artery compression device.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0f74a559-5481-4b81-8b66-db55730b565c 36 fields · synced Jun 1, 2026