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Simpulse

FDA UDI

Class II (US FDA UDI)

by Davol Inc.

Identity

Trade Name
Simpulse FDA UDI
Generic Name
Surgical mist irrigation tip FDA UDI
Device Name
Multi-Jet High Volume Irrigation and Yankauer Suction Tip FDA UDI
Model / Reference
0057681 FDA UDI
Description
Multi-Jet High Volume Irrigation and Yankauer Suction Tip FDA UDI

Identifiers

Catalog Number
0057681 FDA UDI
Primary DI / UDI-DI
00801741010385 FDA UDI
FDA Product Code
FQH FDA UDI
GMDN Term
Surgical mist irrigation tip FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5475 FDA UDI
Commercial Distribution
Not 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

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Davol Inc.

Sources (1)

  • FDA UDI 5d350e97-24ff-44ea-88a3-9e01d3757483 36 fields · synced Jun 8, 2026