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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
Subcutaneous tunneller, single-use FDA UDI
Device Name
IPG Insertion Tool FDA UDI
Model / Reference
23006 FDA UDI
Description
IPG Insertion Tool FDA UDI

Identifiers

Catalog Number
23006 FDA UDI
Primary DI / UDI-DI
00812537034812 FDA UDI
FDA Product Code
GZF FDA UDI
GZB FDA UDI
GMDN Term
Subcutaneous tunneller, single-use 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

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

Category: Subcutaneous tunneller, single-use

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

Similar devices

Also classified as Subcutaneous tunneller, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nalu Medical

Sources (1)

  • FDA UDI 92d8ca02-23da-4215-afbb-a143bc61f41a 36 fields · synced Jun 8, 2026