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Quattrode®

FDA UDI

Class III (US FDA UDI)

by Advanced Neuromodulation Systems

Identity

Trade Name
Quattrode® FDA UDI
Generic Name
Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection FDA UDI
Device Name
Lead 3/4mm, 110 cm FDA UDI
Model / Reference
3141 FDA UDI
Description
Lead 3/4mm, 110 cm FDA UDI

Identifiers

Catalog Number
3141 FDA UDI
Primary DI / UDI-DI
05414734401562 FDA UDI
PMA Number
P010032 FDA UDI
FDA Product Code
LGW FDA UDI
GMDN Term
Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Dimensions & Sizes

Size
Length — 110 Centimeter FDA UDI

Quattrode® by Advanced Neuromodulation Systems — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

P010032 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Advanced Neuromodulation Systems

Sources (1)

  • FDA UDI a20dd7dc-7098-43b7-9c16-445dc1681693 39 fields · synced May 30, 2026