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: Straw Tunneler FDA UDI
Model / Reference: 23007 FDA UDI
Description: Straw Tunneler FDA UDI

Identifiers

Catalog Number: 23007 FDA UDI
Primary DI / UDI-DI: 10812537034833 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

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

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Also classified as Subcutaneous tunneller, single-use.

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Halyard — Avanos Medical, Inc. · Class II
AVANOS — Avanos Medical, Inc. · Class II
Halyard — Avanos Medical, Inc. · Class II
Mainstay Tunneler — MAINSTAY MEDICAL LIMITED · Class III

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Nalu Medical

Sources (1)

FDA UDI 66fa3a99-394c-4c42-9081-902cc2af856d 36 fields · synced Jun 1, 2026