← Back to catalogue

ClosureFast

FDA UDI

Class I (US FDA UDI)

by Covidien LP

Identity

Trade Name
ClosureFast FDA UDI
Generic Name
Intra-arterial needle FDA UDI
Device Name
Arterial Needle,Ultra Thin Wall,19 G (1.067 mm) x 2.75"" (70 mm) FDA UDI
Model / Reference
AN-19G FDA UDI
Description
Arterial Needle,Ultra Thin Wall,19 G (1.067 mm) x 2.75"" (70 mm) FDA UDI

Identifiers

Primary DI / UDI-DI
10884521140172 FDA UDI
FDA Product Code
GDF FDA UDI
GMDN Term
Intra-arterial needle FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

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

Dimensions & Sizes

Size
Length — 2.75 Inch FDA UDI

Category: Intra-arterial needle

A versatile, ultra-thin wall arterial needle suitable for various medical procedures. Learn more about its features and uses.

Similar devices

Also classified as Intra-arterial needle.

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

Manufacturer
Covidien LP

Sources (1)

  • FDA UDI a27e1c33-0020-4b39-82d7-15944c1682bf 35 fields · synced Jul 24, 2026