United States · Bill · S
S. 4098 (109th)
Pediatric Medical Device Safety and Improvement Act of 2006
Introduced
6 December 2006
Last action
6 December 2006 · Introduced
Status
Read twice and referred to the Committee on Health, Education, Labor, and Pensions. (text of measure as introduced: CR S11346-11348)
Sponsors
Sen. Dodd, Christopher J. [D-CT], Sen. DeWine, Mike [R-OH], Sen. Clinton, Hillary Rodham [D-NY]
Subjects
Healthcare
Source updated
15 August 2025
Summary
Pediatric Medical Device Safety and Improvement Act of 2006 - Amends the Federal Food, Drug, and Cosmetic Act to require an application for the approval of a medical device or a product development protocol to include: (1) a description of any pediatric subpopulations that suffer from the disease or condition that the device is intended to treat, diagnose, or cure; and (2) the number of affected pediatric patients. Excludes a medical device distributed pursuant to the humanitarian device exemption from the prohibition that no device be sold for an amount that exceeds the cost of the device if: (1) the device is intended for the treatment or diagnosis of a disease or condition that occurs in pediatric patients; and (2) other specified requirements are met. Requires the Director of the National Institutes of Health (NIH) to designate a contact point to help innovators and physicians access funding for pediatric medical device development. Requires the Secretary of Health and Human Services to award grants for demonstration projects to promote pediatric device development. Includes as a duty of the Office of Pediatric Therapeutics increasing pediatric access to medical devices. Allows the Secretary to require: (1) postmarket surveillance on certain devices that are expected to have significant use in pediatric populations; and (2) a prospective surveillance period of more than 36 months for such devices, as necessary. Requires the Secretary, acting through the Commissioner of Food and Drugs, to establish a publicly accessible database of all studies and surveillance of medical devices. Requires the Secretary to adopt voluntary national standards for medical device coding.
This text is taken from the official record. PoliticalRepo does not editorialize.
Timeline
6 December 2006
Introduced
Sponsor introductory remarks on measure. (CR S11343-11346)
Source: IntroReferral
6 December 2006
Introduced
Introduced in Senate
Source: IntroReferral
6 December 2006
Introduced
Read twice and referred to the Committee on Health, Education, Labor, and Pensions. (text of measure as introduced: CR S11346-11348)
Source: IntroReferral
Votes
No vote records are attached yet.
Versions
- Introduced in Senate · 6 December 2006 · Download file
Documents
3 official files
Introduced in Senate (text)
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Introduced in Senate (text)
Introduced in Senate · EN · 6 December 2006
Introduced in Senate (PDF)
Introduced in Senate · EN · 6 December 2006
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Introduced in Senate
summary · EN · 6 December 2006
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Documentvertaling op verzoek met downloadbare PDF (logo + link naar de officiële bron). Het bronbestand blijft leidend.
Sponsors
- Sen. Dodd, Christopher J. [D-CT] · D · Sponsor
- Sen. DeWine, Mike [R-OH] · R · Sponsor
- Sen. Clinton, Hillary Rodham [D-NY] · D · Cosponsor
- · sshr00 · Standing
Related records
No cross-record relationships stored yet.
Sources
PoliticalRepo is an index and interpretation layer, not the authoritative legal source.
- Official source: https://www.congress.gov/bill/109th-congress/senate-bill/4098
- Open data entity: https://api.congress.gov/v3/bill/109/s/4098
- us · 109-s-4098 · source updated 15 August 2025