AccessGUDID - DEVICE: ATRAMAT (07500142007231)

GUDID

Device Identifier (DI) Information

Brand Name: ATRAMAT
Version or Model: SEDA
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 00723
Company Name: Internacional Farmacéutica, S.A. de C.V.

Primary DI Number: 07500142007231
Issuing Agency: GS1
Commercial Distribution End Date: September 29, 2029
Device Count: 1
Labeler D-U-N-S® Number*: 811313428 *Terms of Use

Device Description: SEDA NEGRA USP 7-0, 45 CM DOBLE AGUJA EE-6 ESPATULADA PREMIUM 6 MM 3/8 CIRCUL

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 Names and Definitions: © Copyright GMDN Agency 2015. Reproduced with Permission from the GMDN Agency.

GMDN Preferred Term Name	GMDN Definition
Silk suture, sterile	A sterile, natural, non-bioabsorbable thread made from raw silk spun by silkworms (typically coated with beeswax or silicone) 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 needle. It provides temporary wound support until the wound sufficiently heals to withstand normal stress. Although classified as a "non-bioabsorbable" material, it may be digested by proteolysis after an extended period of time. This is a single-use device.

GMDN Preferred Term Name

GMDN Definition

Silk suture, sterile

A sterile, natural, non-bioabsorbable thread made from raw silk spun by silkworms (typically coated with beeswax or silicone) 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 needle. It provides temporary wound support until the wound sufficiently heals to withstand normal stress. Although classified as a "non-bioabsorbable" material, it may be digested by proteolysis after an extended period of time. This is a single-use device.

FDA Product Code

[?]

Product Code	Product Code Name
GAP	Suture, Nonabsorbable, Silk

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

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: between 15 and 30 Degrees Celsius
Storage Environment Humidity: between 0 and 65 Percent (%) Relative Humidity

Clinically Relevant Size

[?]

Size Type Text
Length: 6 Millimeter

Device Record Status

Public Device Record Key: 59cb97b3-f629-4cba-930a-27e55995ae59
Public Version Date: March 29, 2018
Public Version Number: 2
DI Record Publish Date: September 27, 2016