Schema first
Every form defines all accepted keys and field descriptions before the agent runs.
Official medical device form hub
Free AI form fillers for medical device submissions
Paste the company and product information you already have. Pi prepares each regulator-specific expected JSON, and a deterministic writer returns an editable draft of the official Word or Excel file.
No source-file uploadOfficial editable templatesMissing facts stay blankFree preliminary draft
Choose an official form
One fixed JSON contract for every regulator form
Each tool has its own field definitions, evidence rules, expected JSON, official template, version note, and deterministic writer mapping.
Brazil · DOCX
ANVISA RDC 751 form filler
Paste product and company information and receive an AI-prepared copy of ANVISA’s Class III and IV medical device petition form.
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Brazil · DOCX
ANVISA classification form filler
Turn pasted company and device facts into a review-ready draft of ANVISA’s official Ficha de Enquadramento V2 Word form.
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Brazil · XLSX
ANVISA model list filler
Paste an unstructured portfolio or product list and download the official ANVISA model-list spreadsheet populated with extracted model names.
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Mexico · DOCX
COFEPRIS registration form filler
Paste applicant, establishment, product, and manufacturer facts and receive a preliminary filled copy of the current COFEPRIS authorizations Word form.
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Evidence bounded
Unsupported facts remain null instead of being inferred from what a typical filing might contain.
Original file output
The final download remains an editable official DOCX or XLSX, not a generic Markdown report.
From draft to submission
Free automation handles transcription. Experts handle regulatory judgment.
A form can be mechanically complete and still use the wrong pathway, classification, technical name, evidence set, manufacturer structure, or current procedure. Pure Global provides global medical device registration support when the work moves from a preliminary draft to a real authority submission.
DJ Fang
MedTech Regulatory Expert
Need help confirming a classification or planning your registration?
Medical device official form filler FAQ
Which medical device forms can the free tool fill?
The first release covers ANVISA’s RDC 751 Class III/IV petition form, ANVISA Ficha de Enquadramento V2, ANVISA’s model-list spreadsheet, and the current COFEPRIS authorizations form fields relevant to device registration.
Can I paste information instead of uploading files?
Yes. Every tool uses a large text box. You can paste prose, email content, copied tables, product specifications, or mixed-language notes.
How does the form remain editable?
The output starts from a stored copy of the official DOCX or XLSX. Pi returns a fixed JSON object, and a deterministic document adapter writes the supported values into that original file.
Are these regulator-approved filing services?
No. They create preliminary editable drafts only. A qualified person must confirm the form version, procedure, data, attachments, signatures, and submission requirements.