Endoscopy Kit - Upper MDKT1A0002A

Trade name

Endoscopy Kit - Upper

Generic name

Endoscopy preparation kit

Model / reference

MDKT1A0002A

Primary DI / UDI-DI

00858276007465

FDA product code

KMJ

GMDN term

Endoscopy preparation kit

Device class

Class I

Regulation number

880.6375

GUDID distribution status

In Commercial Distribution

Category: Endoscopy preparation kit

Other devices filed under FDA product code KMJ (Lubricant, Patient).

• MENTOR LUBRICATING JELLY by Mentor Corp.
• PDI STERILE LUBRICATING JELLY by Nice-Pak Products, LLC
• SANA-LUBE by Huntington Laboratories, Inc.
• DYNACOR LUBRICATION GEL by MEDLINE INDUSTRIES, INC.
• LUBRIGLIDE by Qualis, Inc.
• MODIFIED AMERICAN LUBRICATING JELLY, 2.7 & 5.0 by SPAN-AMERICA MEDICAL SYSTEMS, INC.
• STERILE SALINE SOLUTION by I M, Inc.
• AMERICAN LUBRICATING JELLY STERILE 2.7G & 5G by SPAN-AMERICA MEDICAL SYSTEMS, INC.
• SHEFFIELD PHARMACEUTICALS (STERILE) LUBRIGEL by Sheffield Industries, Div. of Faria, Ltd.
• SPIRUS MEDICAL SURGICAL INSTRUMENT by Spirus Medical, LLC

• Endoscopy Kit - Basic Aux HB DKT1HA0008A

  Class I

  FDA 510(k) K220210 Active Cleared 17 Jun 2022 GUDID on market

• 3-Piece Valve Kit BW01-FUJ3-F7

  Class II

  FDA 510(k) K220210 Active Cleared 17 Jun 2022 GUDID on market

• Active Cord Reusable Bovie AEC-03-08

  Class II

  FDA 510(k) K974793 Active Cleared 19 Mar 1998 GUDID on market

• 5-Piece Valve Kit BW01-FUJ5-F56

  Class II

  FDA 510(k) K220210 Active Cleared 17 Jun 2022 GUDID on market

See all devices from Micro-tech Usa →