AccessGUDID - DEVICE: GENESYS PRESSFT (10845854027868)

GUDID

Device Identifier (DI) Information

Brand Name: GENESYS PRESSFT
Version or Model: NB211H
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: NB211H
Company Name: Conmed Corporation

Primary DI Number: 10845854027868
Issuing Agency: GS1
Commercial Distribution End Date: April 17, 2024
Device Count: 1
Labeler D-U-N-S® Number*: 071595540 *Terms of Use

Device Description: GENESYS PRESS FT 2.1 W/ONE # 2 (5 METRIC) HI-FI SUTURE, HIP

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:	Yes
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?
45061	Tendon/ligament bone anchor, bioabsorbable	A bioabsorbable device designed to be implanted into bone for the attachment of tendons/ligaments/soft tissues either directly or via a suture attached to the device; typically used in arthroscopic or open surgical procedures. This device is available in various designs and sizes and is made of a material that can be chemically degraded and typically absorbed via natural body processes (e.g., a copolymer, metal alloy).	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
MAI	FASTENER, FIXATION, BIODEGRADABLE, SOFT TISSUE

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K121890	000

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 DRY
Storage Environment Temperature: less than 104 Degrees Fahrenheit
Storage Environment Temperature: less than 40 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
Outer Diameter: 2.1 Millimeter

Device Record Status

Public Device Record Key: f2a19eeb-df68-4290-9a35-42a6c19f7ecd
Public Version Date: April 18, 2024
Public Version Number: 6
DI Record Publish Date: October 24, 2015