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Passio Valve Cap Kit PAS-13

by Bearpac Medical, LLC

Passio Valve Cap Kit PAS-13 is a pleural/peritoneal drainage catheterization kit (FDA Class II; FDA product code DWM, Apparatus, Suction, Patient Care) made by Bearpac Medical, LLC, listed in FDA GUDID since 29 Feb 2024 (UDI-DI 00860099001391), 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 Number00860099001391 UDI-DI Date29 Feb 2024ListedStatusListed 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  • Withdrawn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
Passio Valve Cap Kit
Generic name
Pleural/peritoneal drainage catheterization kit, non-medicated
Model / reference
PAS-13
Primary DI / UDI-DI
00860099001391
FDA product code
DWM
GMDN term
Pleural/peritoneal drainage catheterization kit, non-medicated
Device class
Class II
Regulation number
870.5050
GUDID distribution status
In Commercial Distribution

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 Bearpac Medical, LLC

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Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (7, all answered No)