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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
Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wireless connection FDA UDI
Device Name
Stylet (straight, 30 cm) FDA UDI
Model / Reference
23012-030 FDA UDI
Description
Stylet (straight, 30 cm) FDA UDI

Identifiers

Catalog Number
23012-030 FDA UDI
Primary DI / UDI-DI
00812537030197 FDA UDI
FDA Product Code
GZF FDA UDI
GMDN Term
Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wireless connection 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

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

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 30 Centimeter FDA UDI

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

Nalu Medical, Inc. by Nalu Medical — Class II — 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, wireless connection.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nalu Medical

Sources (1)

  • FDA UDI 554f7dad-21a5-4f3b-9887-678c22625832 37 fields · synced May 30, 2026