AccessGUDID - DEVICE: HELMUT ZEPF (EZPF19572120)

GUDID

Device Identifier (DI) Information

Brand Name: HELMUT ZEPF
Version or Model: 19.572.12
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 19.572.12
Company Name: Helmut Zepf Medizintechnik GmbH

Primary DI Number: EZPF19572120
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 320001431 *Terms of Use

Device Description: PROBE BOWMAN, GERMAN SILVER, 13 CM, FIG-1/2, DIAM 0,9 AND 1,1 MM

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	Yes
For Single-Use:	No
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
35252	Fistula probe	A slender, rod-like, hand-held manual surgical instrument made of flexible metal, with a blunt bulbous tip, designed for use in abnormal body passages or communications (fistulas), usually between two internal organs, or leading from an internal organ to an external cavity or to the surface of the body. It is mostly used to explore and/or dilate strictures inside a fistula. This is a reusable device.	Obsolete	false

FDA Product Code

[?]

Product Code	Product Code Name
HXB	PROBE

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: Yes

Sterilization Method [?]
Moist Heat or Steam Sterilization

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: cb4e801f-0e73-48c7-880c-448cf7c5d14f
Public Version Date: December 08, 2022
Public Version Number: 1
DI Record Publish Date: November 30, 2022