Solventum™ Kerramax Care™

Basic Information

• Brand Name: Solventum™ Kerramax Care™
• Primary DI: 00197998276187
• Version / Model: PRD500-050-B50
• Catalog Number: PRD500-050-B50
• Company Name: Solventum US LLC
• Labeler DUNS: 119004140
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 50
• Record Status: Published
• Publish Date: 2026-02-15
• Public Version: 1
• Public Version Date: 2026-02-23
• Public Version Status: New
• Public Device Record Key: 422e96fa-658f-42fa-9a22-17d63d15932d

Device Description

Solventum™ Kerramax Care™ Super-absorbent Dressing, PRD500-050-B50, 4 inx 4 in (10 cm x 10 cm), 50/CAR, 16 CAR/CS, 800/CS

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): No
• Over the Counter (OTC): No
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: No
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: Yes
• PM Exempt: Yes
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: Yes
• Has Expiration Date: Yes
• Has Donation ID: No

Sterilization

• Is Sterile: Yes
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
NAC	Dressing, wound, hydrophilic	General, Plastic Surgery	878.4018	1

GMDN Terms

Code	Name	Definition	Implantable	Status
44970	Exudate-absorbent dressing, non-gel, non-antimicrobial	A wound covering intended to assist in wound healing by absorbing exudate in wounds (e.g., ulcers, burns, surgical wounds, lacerations, abrasions) and often by creating a moist wound-healing environment. It is not in the form of a gel and does not produce a water-absorbent gel upon contact with wound exudates, but may be designed to absorb and remove exudates (e.g., by capillary action); it does not contain an antimicrobial agent, but may include antioxidant properties. The device is available in a variety of forms (e.g., flat sheet/film-like, impregnated pouches, filled sachets, lyophilized matrix, ribbon, rope, foam, liquid, or powder). After application, this device cannot be reused.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Package	00197998276194	GS1	CASE	16	In Commercial Distribution
Primary	00197998276187	GS1
Unit of Use	00197998276019	GS1

Customer Contacts

• Phone: [phone]
• Email: [email protected]