AccessGUDID - DEVICE: LUPINE ORTHOCORD (10886705001095)

GUDID

Device Identifier (DI) Information

Brand Name: LUPINE ORTHOCORD
Version or Model: 210711
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 210711
Company Name: Medos International Sàrl

Primary DI Number: 10886705001095
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 482661753 *Terms of Use

Device Description: LUPINE BR ANCHOR w/ORTHOCORD TCP/PLGA Absorbable Anchor, size 2 (5 metric) braided composite suture, violet 36 Inches (91cm). Size 2 (5 metric) eyelet loop.

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
GAS	Suture, nonabsorbable, synthetic, polyester
MAI	FASTENER, FIXATION, BIODEGRADABLE, SOFT TISSUE
GAM	SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID
GAT	SUTURE, NONABSORBABLE, SYNTHETIC, POLYETHYLENE
HTY	PIN, FIXATION, SMOOTH
MBI	Fastener, fixation, nondegradable, soft tissue
JDR	Staple, fixation, bone

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K040827	000
K070925	000
K150209	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
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: ef8d120a-e4ce-4d1d-a206-6454409faaf3
Public Version Date: April 11, 2025
Public Version Number: 9
DI Record Publish Date: September 01, 2015