FDA.report

CARDINAL HEALTH

Primary DI
50197106964024
Brand
CARDINAL HEALTH
Company
Cardinal Health 200, LLC
Model
SMAHDDCHC3
Catalog number
SMAHDDCHC3
Device description
D C CYSTO PACK
Published
2025-03-07
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Related Records

Product Codes

CodeName
PKFD and C tray

Product Code Classifications

CodeDeviceSpecialtyClass
PKFD And C TrayUnknownN

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
50197106964024PackageGS14In Commercial Distribution
10197106964026PrimaryGS10

GMDN Terms

TermDefinition
Obstetrical/gynaecological surgical procedure kit, non-medicated, single-useA collection of various sterile surgical instruments, dressings/drapes, and materials intended to be used during obstetrical/gynaecological surgery. The kit may be referred to as a procedure pack and is typically comprised of devices that individually are not dedicated to a specific type of obstetrical/gynaecological surgical procedure, but are often supplied together to perform a specific type of obstetrical/gynaecological procedure; it does not contain pharmaceuticals. This is a single-use device.

Sterilization Methods

Method

Regulatory Flags

DUNS number
961027315
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
true
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
true
Sterilization required before use
false

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