← Back to catalogue

Arista

FDA UDI

Class III (US FDA UDI)

by Davol Inc.

Identity

Trade Name
ARISTA FDA UDI
Generic Name
Atomizing surgical topical solution applicator FDA UDI
Device Name
Arista AH FlexiTip Applicator, 14 cm (5.5 in) FDA UDI
Model / Reference
AM0004 FDA UDI
Description
Arista AH FlexiTip Applicator, 14 cm (5.5 in) FDA UDI

Identifiers

Catalog Number
AM0004 FDA UDI
Primary DI / UDI-DI
10801741044066 FDA UDI
FDA Product Code
LMG FDA UDI
GMDN Term
Atomizing surgical topical solution applicator FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
878.4490 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

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 14 Centimeter FDA UDI

Category: Atomizing surgical topical solution applicator

Arista by Davol Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Atomizing surgical topical solution applicator.

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 71cc45e6-0638-462b-958e-d2c44bd699ad 36 fields · synced May 30, 2026