AccessGUDID - DEVICE: QUICKANCHOR ORTHOCORD (10886705001835)

GUDID

Device Identifier (DI) Information

Brand Name: QUICKANCHOR ORTHOCORD
Version or Model: 212035
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 212035
Company Name: Medos International Sàrl

Primary DI Number: 10886705001835
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 482661753 *Terms of Use

Device Description: Mini QUICKANCHOR Plus (Number 2/0 Suture) Size 2/0 (3 metric) ORTHOCORD braided composite suture, 18 Inches (45cm), double-armed V-5 needles and 2.0 x 9.7mm drill bit, with disposable inserter.

Device Characteristics

What MRI safety information does the labeling contain?	MR Conditional
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?
45062	Tendon/ligament bone anchor, non-bioabsorbable	A non-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 cannot be chemically degraded or absorbed via natural body processes [e.g., titanium (Ti)].	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
HWC	Screw, fixation, bone
MAI	FASTENER, FIXATION, BIODEGRADABLE, SOFT TISSUE
JDR	STAPLE, FIXATION, BONE

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K071257	000
K992487	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
Handling Environment Temperature: less than 25 Degrees Celsius
Handling Environment Temperature: less than 77 Degrees Fahrenheit
Storage Environment Temperature: less than 77 Degrees Fahrenheit
Storage Environment Temperature: less than 25 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: cf3ae249-4e89-49f6-ab6b-704571e6d940
Public Version Date: March 25, 2025
Public Version Number: 6
DI Record Publish Date: September 01, 2015