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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
Peripheral nerve-block sharp needle FDA UDI
Device Name
PROLONG* Continuous Nerve Block Set FDA UDI
Model / Reference
32774 FDA UDI
Description
PROLONG* Continuous Nerve Block Set FDA UDI

Identifiers

Catalog Number
PL18050TGC FDA UDI
Primary DI / UDI-DI
00193494327743 FDA UDI
FDA Product Code
CAZ FDA UDI
CAC FDA UDI
BSO FDA UDI
BSP FDA UDI
GMDN Term
Peripheral nerve-block sharp needle FDA UDI

Classification

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

No

FDA UDI

Dimensions & Sizes

Size
Needle Gauge — 18 Gauge FDA UDI

Category: Peripheral nerve-block sharp needle

PROLONG* Continuous Nerve Block Set by Avanos Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral nerve-block sharp needle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a5e36675-41f6-4f3f-890d-bf536c18a305 36 fields · synced Jun 9, 2026