AccessGUDID - DEVICE: Sil-Select Plus (54119670001734)

GUDID

Device Identifier (DI) Information

Brand Name: Sil-Select Plus
Version or Model: SIP008
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number:
Company Name: Fertipro NV

Primary DI Number: 54119670001734
Issuing Agency: GS1
Commercial Distribution End Date: September 30, 2017
Device Count: 1
Labeler D-U-N-S® Number*: 373904101 *Terms of Use

Device Description: Sil-Select Plus™ (SIP008) This kit contains the following product codes: 8 x 2.5 ml Sil-Select Plus Upper Layer 8 x 2.5ml Sil-Select Plus Lower Layer 8 x 2.5 ml washing/insemination medium Sil-Select Plus™ is a solution of silane-coated sicila particles in a chemically defined, balanced salts solution with HEPES (pH buffer). Sil-Select Plus has a 18 month shelf life from date of manufacturer For the latest version of the intructions for use and MSDS, visit our product page on the FertiPro's website (www.fertipro.com)

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:	No
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?
44046	IVF medium	A solution that provides a physiological environment for the retrieval, culture, maintenance, transfer, and/or storage of human sperm, harvested oocytes (eggs), and/or resulting embryos associated with the method of in vitro fertilization (IVF). The solution typically contains various combinations of salts, carbohydrates, amino acids, enzymes, hormones, albumin, vitamins, and/or drugs (e.g., antibiotics). This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
MQL	Media, Reproductive

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K053494	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: between 2 and 8 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 7e8c5090-2aed-4d5e-a6a5-fdc057397a8c
Public Version Date: June 24, 2024
Public Version Number: 3
DI Record Publish Date: September 29, 2017