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Streamline™

FDA UDI

Class II (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
STREAMLINE™ FDA UDI
Generic Name
Transthoracic pacing lead FDA UDI
Device Name
WIRE 6491F TEMP PACE PED 12PK 26L FDA UDI
Model / Reference
6491F FDA UDI
Description
WIRE 6491F TEMP PACE PED 12PK 26L FDA UDI

Identifiers

Primary DI / UDI-DI
00643169310070 FDA UDI
FDA Product Code
LDF FDA UDI
GMDN Term
Transthoracic pacing lead FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.3680 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Transthoracic pacing lead

Streamline™ by Medtronic, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Transthoracic pacing lead.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI 09a281e2-b06d-4200-bf8f-b0c4d036169d 35 fields · synced May 30, 2026