AccessGUDID - DEVICE: Sutralene (M583P540151RC1)

GUDID

Device Identifier (DI) Information

Brand Name: Sutralene
Version or Model: P540151RC
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: VISIONARY MEDICAL SUPPLIES INC

Primary DI Number: M583P540151RC1
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 111585795 *Terms of Use

Device Description: 5-0 Suture USP / Thread Specifications: Polypropylene, Blue Monofilament, 28 inch (70 cm) / Needle Specifications: RC-130-15, Reverse Cutting, 3/8 circle (140 degrees), length 13.1 mm, wire 0.38 mm / # of needles: single arm

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?
13909	Polyolefin/fluoropolymer suture, monofilament	A single-strand (monofilament), synthetic, non-bioabsorbable thread made of a polyolefin (e.g., polypropylene, polyethylene) or fluoropolymer (e.g., polytetrafluoroethylene, polyvinylidene fluoride) intended to join (i.e., approximate) the edges of a soft-tissue wound or incision by stitching or to ligate soft tissues; it may include an attached disposable device(s) [e.g., needle, passer] intended to facilitate suture application. The thread provides temporary wound support until the wound sufficiently heals to withstand normal stress. It is not a barbed suture and does not include antimicrobial agents/materials. This is a single-use device.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
GAW	Suture, Nonabsorbable, Synthetic, Polypropylene

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K070243	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
Angle: 140 degree
Device Size Text, specify: 5-0 USP
Outer Diameter: 0.38 Millimeter
Length: 13.1 Millimeter
Length: 70 Centimeter

Device Record Status

Public Device Record Key: 7665963f-f5c8-4cb9-a8fd-af7889050ee4
Public Version Date: June 02, 2023
Public Version Number: 6
DI Record Publish Date: June 14, 2016