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Simpulse

FDA UDI

Class II (US FDA UDI)

by Davol Inc.

Identity

Trade Name
SIMPULSE FDA UDI
Generic Name
Disposable surgical irrigation/aspiration system FDA UDI
Device Name
The Simpulse SOLO System with Ultrex Retractable Splash Shield Tip FDA UDI
Model / Reference
0067500 FDA UDI
Description
The Simpulse SOLO System with Ultrex Retractable Splash Shield Tip FDA UDI

Identifiers

Catalog Number
0067500 FDA UDI
Primary DI / UDI-DI
00801741010170 FDA UDI
FDA Product Code
FQH FDA UDI
GMDN Term
Disposable surgical irrigation/aspiration system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5475 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: Disposable surgical irrigation/aspiration system

Simpulse by Davol Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Disposable surgical irrigation/aspiration system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Davol Inc.

Sources (1)

  • FDA UDI fa40ad3b-b306-4789-9672-8d8a4b08d621 37 fields · synced Jun 6, 2026