PROLONG* Continuous Nerve Block Set

FDA UDI

Class II (US FDA UDI)

by Avanos Medical, Inc.

Identity

Trade Name: PROLONG* Continuous Nerve Block Set FDA UDI
Generic Name: Subcutaneous tunneller, single-use FDA UDI
Device Name: PROLONG* Continuous Nerve Block Set FDA UDI
Model / Reference: 32771 FDA UDI
Description: PROLONG* Continuous Nerve Block Set FDA UDI

Identifiers

Catalog Number: PL19100GC FDA UDI
Primary DI / UDI-DI: 00193494327712 FDA UDI
FDA Product Code: CAZ FDA UDI
CAC FDA UDI
BSP FDA UDI
BSO FDA UDI
GMDN Term: Subcutaneous tunneller, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5140 FDA UDI
868.5830 FDA UDI
868.5150 FDA UDI
868.5120 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

Yes

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

FDA UDI

Dimensions & Sizes

Size: Needle Gauge — 19 Gauge FDA UDI

Category: Subcutaneous tunneller, single-use

PROLONG* Continuous Nerve Block Set by Avanos Medical, Inc. — 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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CODMAN® — Integra LifeSciences Production Corporation · Class I
CODMAN® — Integra LifeSciences Production Corporation · Class I
Natus® — Natus Medical Incorporated · Class I

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: Avanos Medical, Inc.

Sources (1)

FDA UDI 68ac508d-34c2-4d09-803e-3434932c0480 36 fields · synced Jun 9, 2026