← Back to catalogue

Introducer Needle

FDA UDI

Class II (US FDA UDI)

by Bard Access Systems, Inc.

Identity

Trade Name
Introducer Needle FDA UDI
Generic Name
Vascular catheter introduction needle FDA UDI
Device Name
SecLoc,INTRO 18Gx2.75 FDA UDI
Model / Reference
S03118-275 FDA UDI
Description
SecLoc,INTRO 18Gx2.75 FDA UDI

Identifiers

Catalog Number
S03118-275 FDA UDI
Primary DI / UDI-DI
10801741075336 FDA UDI
FDA Product Code
DYB FDA UDI
GMDN Term
Vascular catheter introduction needle FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1340 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Needle Gauge — 18 Gauge FDA UDI
Length — 2.75 Inch FDA UDI

Category: Vascular catheter introduction needle

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

Similar devices

Also classified as Vascular catheter introduction 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

Sources (1)

  • FDA UDI 3f207746-35d3-4eda-b163-0e290f22b9c6 36 fields · synced Jun 9, 2026