AccessGUDID - DEVICE: ATRAMAT (07500142056420)

GUDID

Device Identifier (DI) Information

Brand Name: ATRAMAT
Version or Model: NYLON
Commercial Distribution Status: In Commercial Distribution
Catalog Number: PU6042-N
Company Name: Internacional Farmacéutica, S.A. de C.V.

Primary DI Number: 07500142056420
Issuing Agency: GS1
Commercial Distribution End Date: December 31, 2040
Device Count: 1
Labeler D-U-N-S® Number*: 811313428 *Terms of Use

Device Description: ATRAMAT NYLON SURGICAL SUTURE BLACK USP 2-0 EP 3, 75 CM NEEDLE PU-60 PREMIUM STRAIGHT CUTTING 60 MM STRAIGHT NYLON NEGRO USP 2-0, 75 CM AGUJA PU-60 RECTA CORTANTE PREMIUM 60 MM RECTA

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):	No
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?
38000	Nylon suture, non-bioabsorbable, monofilament	A single-strand (monofilament), synthetic, non-bioabsorbable thread made of nylon (a polyamide polymer) 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. 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
GAR	Suture, Nonabsorbable, Synthetic, Polyamide

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K905286	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: between 15 and 30 Degrees Celsius
Handling Environment Humidity: between 0 and 65 Percent (%) Relative Humidity

Clinically Relevant Size

[?]

Size Type Text
Length: 60 Millimeter
Device Size Text, specify: SUTURE BLACK
Device Size Text, specify: RECTA
Device Size Text, specify: ATRAMAT NYLON
Device Size Text, specify: USP 2-0

Device Record Status

Public Device Record Key: 261e3973-4025-49fb-9131-e48d903a2b38
Public Version Date: February 05, 2021
Public Version Number: 6
DI Record Publish Date: September 28, 2016