AccessGUDID - DEVICE: RZ Medizintechnik GmbH (04049197355308)

GUDID

Device Identifier (DI) Information

Brand Name: RZ Medizintechnik GmbH
Version or Model: 600-080-200
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 600-080-200
Company Name: RZ-Medizintechnik GmbH

Primary DI Number: 04049197355308
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 312953227 *Terms of Use

Device Description: Davis Sterilizing Forceps 20.0cm, 8"

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):	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?
11792	Sterilizer transfer forceps	A hand-held, scissors-like, manual surgical instrument whose blades, distal to the pivot point, form open circles, loops, or ellipses designed to grasp and handle sterile instruments, packages, or implants, especially directly from a sterilizer. It is typically made of high-grade stainless steel. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
MDM	INSTRUMENT, MANUAL, SURGICAL, GENERAL USE

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: 571e8bc9-5076-401e-b0ac-b55bec6ebf68
Public Version Date: July 04, 2024
Public Version Number: 1
DI Record Publish Date: June 26, 2024