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Powerforma®

FDA UDI

Class II (US FDA UDI)

by Medtronic Xomed, Inc.

Identity

Trade Name
POWERFORMA® FDA UDI
Generic Name
Surgical irrigation tubing set, single-use FDA UDI
Device Name
TUBING 1895520 5PK PWRFORMA TO XPS IRRIG FDA UDI
Model / Reference
1895520 FDA UDI
Description
TUBING 1895520 5PK PWRFORMA TO XPS IRRIG FDA UDI

Identifiers

Primary DI / UDI-DI
20681490049133 FDA UDI
510(k) Number
K002224 FDA UDI
FDA Product Code
ERL FDA UDI
GMDN Term
Surgical irrigation tubing set, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4250 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical irrigation tubing set, single-use

Powerforma® by Medtronic Xomed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ed5d2ee1-894a-4afe-9371-4ab2ebe181b1 35 fields · synced Jun 1, 2026