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ARS Long

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
ARS Long FDA UDI
Generic Name
Laparoscopic access cannula, single-use FDA UDI
Device Name
AirSeal 8 mm Cannula Cap and Obturator with Bladeless Optical Tip Compatible with Intuitive da Vinci Xi and da Vinci X 8 mm Instrument Cannula, Long Length FDA UDI
Model / Reference
iAS8-dVL FDA UDI
Description
AirSeal 8 mm Cannula Cap and Obturator with Bladeless Optical Tip Compatible with Intuitive da Vinci Xi and da Vinci X 8 mm Instrument Cannula, Long Length FDA UDI

Identifiers

Catalog Number
iAS8-dVL FDA UDI
Primary DI / UDI-DI
10845854084137 FDA UDI
510(k) Number
K211104 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Laparoscopic access cannula, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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
Sterilization Method
Radiation Sterilization FDA UDI

Category: Laparoscopic access cannula, single-use

ARS Long by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laparoscopic access cannula, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 24f158a4-9ca3-4d07-b62a-453f918bfea3 37 fields · synced May 31, 2026