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Cardinal Health SBA30MRPRD

by Cardinal Health 200, LLC

Cardinal Health SBA30MRPRD is a Class II device made by Cardinal Health 200, LLC, listed in FDA GUDID since 30 Apr 2021 (UDI-DI 10195594011505), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10195594011505 UDI-DI Date30 Apr 2021ListedStatusListed 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  • Withdrawn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
Cardinal Health
Generic name
General surgical procedure kit, medicated
Model / Ref / Catalog
SBA30MRPRD
Description
MINOR LAP W CHLORAPREP
Primary DI / UDI-DI
10195594011505
FDA product code
LRO
GMDN term
General surgical procedure kit, medicated
Device class
Class II
Regulation number
878.4370
GUDID distribution status
In Commercial Distribution

Related devices

Category: General surgical procedure kit, medicated

Other devices from Cardinal Health 200, LLC

See all devices from Cardinal Health 200, LLC →

Properties

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