DEVICE: CARDINAL HEALTH (10885380133688)
Device Identifier (DI) Information
CARDINAL HEALTH
C-SG44S
In Commercial Distribution
C-SG44S
Cardinal Health 200, LLC
C-SG44S
In Commercial Distribution
C-SG44S
Cardinal Health 200, LLC
Post-Op Gauze Sponges 4 x 4in.(10.2 x 10.2cm)
Nonwoven with Cellulose Center Sterile.
Sterilized Using Ethylene Oxide. Single Use Only.
Not Made with Natural Rubber Latex. Store in a
Cool, Dry Place.
Device Characteristics
Labeling does not contain MRI Safety Information | |
No | |
Yes | |
Yes | |
No | |
Yes | |
No | |
No | |
No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
---|---|---|---|---|
44971 | General-purpose surgical sponge |
A non-medicated cushion-like mass made of absorbent materials (e.g., woven gauze, cotton, cellulose) primarily intended to be used inside the body, on a surgical incision or applied to internal organs or structures to control bleeding, absorb fluid, or protect organs or structures from abrasion, drying, or contamination during a procedure; also referred to as a laparotomy sponge or cottonoid pad/pattie, it may also be used for prepping the patient. It does not contain special features to help detect gossypiboma (sponge left inside patient) [i.e., it is not radiopaque]. This is a single-use device.
|
Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
NAB | Gauze / sponge,nonresorbable for external use |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
---|---|
Premarket Submission Number Not Available/Not Released |
Sterilization
Storage and Handling
[?]Storage and Handling |
---|
No storage/handling found |
Clinically Relevant Size
[?]Size Type Text |
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No Device Sizes |
Device Record Status
d6c7d267-8707-4843-aa48-a57dacaff489
June 28, 2024
3
June 19, 2019
June 28, 2024
3
June 19, 2019
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
---|---|---|---|---|---|
20885380133685 | 25 | 10885380133688 | 2025-12-30 | In Commercial Distribution | BOX |
50885380133686 | 24 | 20885380133685 | 2025-12-30 | In Commercial Distribution | CASE |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
---|---|
No Secondary DIs found |
Unit of Use DI
[?]
Unit of Use DI Number:
00885380133681
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
No Customer Contact currently defined