Probe-Umb

Generic name

Abdominal/ENT/orthopaedic surgical probe, single-use

Model / reference

PROBE-UMB

Primary DI / UDI-DI

00858778006850

FDA product code

KDC

GMDN term

Abdominal/ENT/orthopaedic surgical probe, single-use

Device class

Class I

Regulation number

878.4800

GUDID distribution status

In Commercial Distribution

Category: Abdominal/ENT/orthopaedic surgical probe, single-use

Other devices filed under FDA product code KDC (Instrument, Surgical, Disposable).

• Scanlan® SUTURE BOOT™ Instrument Jaw Covers 1001-516 by SCANLAN INTERNATIONAL INC
• PEDIATRIC SUCKER by 3M Health Care, Sarns
• HOOK PROBE by Euro-Med Intl.
• Y-TYPE BLOOD SET by Abbott Laboratories
• DRAVON T CLAMP by Dravon Medical Inc
• SUTURE REMOVAL SET, STERILE by Lukens Corp.
• T-Clamp T-200/25 by Dravon Medical Inc
• SPONGE COUNTER BAGS by Medicare Industries, Inc.
• PLASTIC THUMB FORCEPS by Medcare Products
• SAFETY PINS & RUBBER BANDS by Ormed Mfg., Inc.

• Medela ENSI4050

  Class II

  FDA 510(k) K090559 Active Cleared 4 May 2009 GUDID on market

• S1FTS6.5-Eo

  Class II

  FDA 510(k) K090559 Active Cleared 4 May 2009 GUDID on market

• S1UVC-6540

  Class II

  FDA 510(k) K091214 Active Cleared 25 Sep 2009 GUDID on market

• Medela ENSI-90-50

  Class II

  FDA 510(k) K090559 Active Cleared 4 May 2009 GUDID on market

See all devices from Footprint Medical Inc. →