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Pisces-Quad Plus ™

FDA UDI

Class III (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
PISCES-QUAD PLUS ™ FDA UDI
Generic Name
Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection FDA UDI
Device Name
LEAD 3888-33 PSCES4+ 33CM BLUTRQ EMN FWU FDA UDI
Model / Reference
3888-33 FDA UDI
Description
LEAD 3888-33 PSCES4+ 33CM BLUTRQ EMN FWU FDA UDI

Identifiers

Primary DI / UDI-DI
00643169887893 FDA UDI
PMA Number
P840001 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
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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection

Pisces-Quad Plus ™ by Medtronic, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI c70dbcda-d045-4afe-afde-107c019e24b9 35 fields · synced May 31, 2026