← Back to catalogue

Simpulse

FDA UDI

Class II (US FDA UDI)

by Davol Inc.

Identity

Trade Name
Simpulse FDA UDI
Generic Name
Surgical instrument guard, single-use FDA UDI
Device Name
Simpulse Suction Irrigator Splash Shield FDA UDI
Model / Reference
0037640 FDA UDI
Description
Simpulse Suction Irrigator Splash Shield FDA UDI

Identifiers

Catalog Number
0037640 FDA UDI
Primary DI / UDI-DI
00801741010347 FDA UDI
FDA Product Code
FQH FDA UDI
GMDN Term
Surgical instrument guard, single-use 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

Dimensions & Sizes

Size
Outer Diameter — 6.5 Inch FDA UDI

Category: Surgical instrument guard, single-use

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

Similar devices

Also classified as Surgical instrument guard, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Davol Inc.

Sources (1)

  • FDA UDI 4655d7be-bc2b-4170-be99-b1ddfa3f0832 37 fields · synced May 30, 2026