AccessGUDID - DEVICE: ERBE (04050147012929)

GUDID

Device Identifier (DI) Information

Brand Name: ERBE
Version or Model: 20325-222
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 20325-222
Company Name: Erbe Elektromedizin GmbH

Primary DI Number: 04050147012929
Issuing Agency: GS1
Commercial Distribution End Date: December 02, 2021
Device Count: 1
Labeler D-U-N-S® Number*: 316116623 *Terms of Use

Device Description: Endoscopy Pump Tubing/ Cap Set

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":	No
For Single-Use:	No
Prescription Use (Rx):	Yes
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?
46102	Surgical irrigation tubing set, single-use	A collection of flexible, noninvasive, single-lumen tubing and associated items intended to provide a conduit to deliver a sterile irrigation solution (e.g., saline) from its source (e.g., gravity feed bag, feed pump) to a surgical cannula (not included) during a surgical procedure (endoscopy, laparoscopy); it is not intended to navigate through an anatomical lumen. The tubing set includes devices such as clamps, filters, spikes, and Y-piece connectors, and may in addition include an integrated manual pump (e.g., a squeeze bulb) or handpiece. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
OCX	endoscopic irrigation/suction system

FDA Premarket Submission

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

Device Exempt from Premarket Submission: No CLOSE

Sterilization

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

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Special Storage Condition, Specify: Keep away from heat and direct sunlight
Special Storage Condition, Specify: Keep dry

Clinically Relevant Size

[?]

Size Type Text
Length: 2.900 Meter

Device Record Status

Public Device Record Key: 0c21b0bd-3a3f-41e3-b910-fc4b92f6688d
Public Version Date: December 14, 2021
Public Version Number: 8
DI Record Publish Date: December 16, 2016

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
04050147013445	5	04050147013438	2021-12-02	Not in Commercial Distribution	Level: 2
04050147013438	10	04050147012929	2021-12-02	Not in Commercial Distribution	Level: 1