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PeritX 90-2020

by Bard Peripheral Vascular

PeritX 90-2020 is a Class II device made by Bard Peripheral Vascular, listed in FDA GUDID since 23 Jan 2025 (UDI-DI 00801741230639), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00801741230639 UDI-DI Date23 Jan 2025ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
PeritX
Generic name
Pleural/peritoneal drainage catheterization kit, non-medicated
Model / Ref / Catalog
90-2020
Primary DI / UDI-DI
00801741230639
FDA product code
PNG
GMDN term
Pleural/peritoneal drainage catheterization kit, non-medicated
Device class
Class II
Regulation number
876.5630
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 2 Liter

Related devices

Category: Pleural/peritoneal drainage catheterization kit

Similar devices in this category

Other devices filed under Pleural/peritoneal drainage catheterization kit.

Other devices from Bard Peripheral Vascular

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Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (8, all answered No)