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Get the free DoC for Coated VICRYL PLUS Suture

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Regulatory Affairs Submission Declaration of Conformity DoC for Coated VICRYL PLUS Suture100146795 | Rev: 14DECLARATION OF CONFORMITY Manufacturers Name:Ethicon, Inc.Manufacturers Address:Route 22 West PO Box 151 Somerville, New Jersey 088760151 USAAuthorized Representative:Johnson & Johnson Medical GmbH RobertKochStrasse 1 Norderstedt 22851 GermanyProduct:Coated VICRYL Plus Antibacterial (Polyglactin 910) Sterile Synthetic Absorbable SutureProduct Code(s)/Product Range
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01
Gather necessary patient information including name, ID, and procedure details.
02
Obtain the appropriate form for coated vicryl documentation.
03
Fill in the date and time of the procedure at the top of the document.
04
Specify the type and size of coated vicryl used.
05
Document the location of the wound or surgical site.
06
Note any relevant observations during the procedure.
07
Include the name and signature of the healthcare provider performing the procedure.
08
Review the completed document for accuracy before submission.

Who needs doc for coated vicryl?

01
Surgeons performing surgeries involving sutures.
02
Nurses involved in patient care and documentation.
03
Healthcare administrators managing surgical records.
04
Regulatory bodies requiring medical documentation for audits.
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The doc for coated vicryl refers to the documentation required for coated vicryl sutures, which are absorbable sutures made from braided polyglycolic acid and coated to improve handling characteristics and reduce tissue drag.
Healthcare providers or facilities that use coated vicryl sutures are typically required to file the documentation. This can include surgeons, hospitals, and outpatient surgical centers.
To fill out the doc for coated vicryl, providers must provide accurate details on the type, size, and quantity of the sutures used, along with patient information and the surgical procedure performed.
The purpose of the doc for coated vicryl is to ensure traceability, compliance with medical standards, and documentation in surgical records for quality assurance and accountability.
The information that must be reported includes the product code, lot number, expiration date, the surgeon's name, patient identification, surgical site, and any adverse events related to the use of the sutures.
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