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Nalu Medical, Inc.

FDA UDI

Class II (US FDA UDI)

by Nalu Medical

Identity

Trade Name
Nalu Medical, Inc. FDA UDI
Generic Name
Analgesic spinal cord electrical stimulation system FDA UDI
Device Name
Lead Kit (8 contact, 40 cm) FDA UDI
Model / Reference
72001-US FDA UDI
Description
Lead Kit (8 contact, 40 cm) FDA UDI

Identifiers

Catalog Number
72001-US FDA UDI
Primary DI / UDI-DI
00812537033617 FDA UDI
FDA Product Code
GZF FDA UDI
GZB FDA UDI
GMDN Term
Analgesic spinal cord electrical stimulation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5870 FDA UDI
882.5880 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

Yes

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 Conditional FDA UDI

Dimensions & Sizes

Size
Length — 40 Centimeter FDA UDI

Category: Analgesic spinal cord electrical stimulation system

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

Similar devices

Also classified as Analgesic spinal cord electrical stimulation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nalu Medical

Sources (1)

  • FDA UDI e57d0ac4-86b5-44da-a297-bce11e9cd98d 37 fields · synced May 30, 2026