AccessGUDID - DEVICE: COR-KNOT® (00850200006100)

GUDID

Device Identifier (DI) Information

Brand Name: COR-KNOT®
Version or Model: 030800
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 030800
Company Name: LSI Solutions, Inc.

Primary DI Number: 00850200006100
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 2
Labeler D-U-N-S® Number*: 603420183 *Terms of Use

Device Description: COR-KNOT® MIS DEVICE KIT

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?
61353	Suture clasp, non-bioabsorbable	A small, sterile, implantable fastening device designed to secure the ends of a suture as an alternative to tying a knot, for approximation of soft tissue and/or prosthetic materials during a surgical procedure. It is made of non-bioabsorbable materials [e.g., titanium (Ti)] and is typically implanted with a dedicated applicator.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
HCF	Instrument, Ligature Passing And Knot Tying

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K100593	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
Length: 31 Centimeter

Device Record Status

Public Device Record Key: b6b568e5-3f5e-4396-a6df-33e409a90196
Public Version Date: November 10, 2022
Public Version Number: 6
DI Record Publish Date: May 12, 2016

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
10850200006107	6	00850200006100		In Commercial Distribution	Case

Secondary DI

[?]

Issuing Agency [?]	Secondary DI Number
No Secondary DIs found

Unit of Use DI

[?]

Unit of Use DI Number: 40850200006108 CLOSE

Direct Marking (DM)

[?]

Device Subject to Direct Marking (DM), but Excepted: No
DM DI Different from Primary DI: No
DM DI Number: None
CLOSE

Production Identifier(s) in UDI

[?]

Lot or Batch Number: Yes
Serial Number: No
Expiration Date: Yes
Manufacturing Date: No
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: +1(866)575-3493
Email: regulatorydpt@lsisolutions.com

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