AccessGUDID - DEVICE: OMNISPAN ORTHOCORD (10886705010042)

GUDID

Device Identifier (DI) Information

Brand Name: OMNISPAN ORTHOCORD
Version or Model: 228142
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 228142
Company Name: Medos International Sàrl

Primary DI Number: 10886705010042
Issuing Agency: GS1
Commercial Distribution End Date: May 31, 2024
Device Count: 1
Labeler D-U-N-S® Number*: 482661753 *Terms of Use

Device Description: OMNISPAN MENISCAL REPAIR SYSTEM / 27 Degrees ORTHOCORD Violet braided composite suture, Size 2-0, (2) PEEK Backstops, and 27 Degrees (1) Curved Needle

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
MBI	FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE
NEW	Suture, surgical, absorbable, polydioxanone
HTY	PIN, FIXATION, SMOOTH
MAI	Fastener, fixation, biodegradable, soft tissue
JDR	Staple, fixation, bone
GAT	Suture, nonabsorbable, synthetic, polyethylene

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K092836	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
Storage Environment Temperature: less than 77 Degrees Fahrenheit
Storage Environment Temperature: less than 25 Degrees Celsius
Handling Environment Temperature: less than 25 Degrees Celsius
Handling Environment Temperature: less than 77 Degrees Fahrenheit

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: a5039766-4826-42c8-abef-bf7d1cf55c49
Public Version Date: March 25, 2025
Public Version Number: 8
DI Record Publish Date: September 01, 2015