Covidien 777702

• FDA 510(k) K042572 decided 5 Nov 2004 Active
• FDA GUDID UDI-DI 30884521000272 listed 24 Sep 2016 Listed

1. 5 Nov 2004 Cleared FDA 510(k) K042572
2. 24 Sep 2016 Listed FDA GUDID 30884521000272

Trade name

Covidien

Generic name

Exhaled-gas oesophageal intubation detector

Model / Ref / Catalog

777702

Primary DI / UDI-DI

30884521000272

FDA product code

KNT

GMDN term

Exhaled-gas oesophageal intubation detector

Device class

Class II

Regulation number

876.5980

GUDID distribution status

In Commercial Distribution

Category: Medical device adhesive

Other devices filed under FDA product code KNT (TUBES, GASTROINTESTINAL (AND ACCESSORIES)).

• AMT LOW-PROFILE TRANSGASTRIC-JEJUNAL FEEDING TUBE KIT by Applied Medical Technology, Inc.
• ARGYLE DUO-TUBE by Sherwood Medical Co.
• Standard Bougie, 38 Fr. and Hand Pump by Standard Bariatrics
• TubeClear System by ACTUATED MEDICAL, INC.
• LOW PROFILE PASSPORT PUSH & PULL KITS & PEG TUBE by Wilson-Cook Medical, Inc.
• ENDOVIVE INITIAL PLACEMENT PEG KIT, DIRECT PEJ KIT, AND PEG SAFETY KIT by Boston Scientific
• PROCON by Healthcare Management Systems
• PERCUTANEOUS GASTROSTOMY TUBE by Mount Carmel Mercy Hospital
• PERISTEEN ANAL IRRIGATION SYSTEM, PERISTEEN ANAL IRRIGATION ACCESSORY UNIT, PERISTEEN ANAL IRRIGATION RECTAL CATHETER by Coloplast A/S
• RADIUS LOW PROFILE GASTROSTOMY TUBE KIT by Radius Intl., Inc.

• Curity 8047G

  Class I

  GUDID on market

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