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Pipeline

FDA UDI

Class I (US FDA UDI)

by Depuy Spine, Inc.

Identity

Trade Name
PIPELINE FDA UDI
Generic Name
Orthopaedic guidewire, reusable FDA UDI
Device Name
PIPELINE LS ACCESS SYSTEM GUIDEWIRE, SHARP 2mm FDA UDI
Model / Reference
287105001 FDA UDI
Description
PIPELINE LS ACCESS SYSTEM GUIDEWIRE, SHARP 2mm FDA UDI

Identifiers

Catalog Number
287105001 FDA UDI
Primary DI / UDI-DI
10705034217567 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic guidewire, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic guidewire, reusable

Pipeline by Depuy Spine, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic guidewire, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Depuy Spine, Inc.

Sources (1)

  • FDA UDI 787a3aa7-01e2-449a-bc7f-cbc11f0bd0d7 35 fields · synced May 30, 2026