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Werewolf Irrigation Tube Set

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
WEREWOLF IRRIGATION TUBE SET FDA UDI
Generic Name
Surgical irrigation tubing set, single-use FDA UDI
Device Name
WEREWOLF ENT SALINE TUBING FDA UDI
Model / Reference
72290135 FDA UDI
Description
WEREWOLF ENT SALINE TUBING FDA UDI

Identifiers

Catalog Number
72290135 FDA UDI
Primary DI / UDI-DI
00885556699935 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Surgical irrigation tubing set, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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

No

FDA UDI

Category: Surgical irrigation tubing set, single-use

Werewolf Irrigation Tube Set by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical irrigation tubing set, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 039f9c80-f746-40e6-97d5-28e2bea3b70d 35 fields · synced Jun 8, 2026