← Back to catalogue

Nalu Medical, Inc.

FDA UDI

Class II (US FDA UDI)

by Nalu Medical

Identity

Trade Name
Nalu Medical, Inc. FDA UDI
Generic Name
Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system lead FDA UDI
Device Name
Trial Lead (4 contact, 40 cm) FDA UDI
Model / Reference
12009-040-US FDA UDI
Description
Trial Lead (4 contact, 40 cm) FDA UDI

Identifiers

Catalog Number
12009-040-US FDA UDI
Primary DI / UDI-DI
00812537036236 FDA UDI
FDA Product Code
GZF FDA UDI
GMDN Term
Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system lead FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5870 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Length — 40 Centimeter FDA UDI

Category: Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system lead

Nalu Medical, Inc. by Nalu Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system lead.

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

Manufacturer
Nalu Medical

Sources (1)

  • FDA UDI 8366daad-e097-4741-87c8-7f120e03a7e7 37 fields · synced May 30, 2026