FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE

DI: 10080196392278 · Model: SDKKLPR · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
MEDLINE
Primary DI
10080196392278
Version / Model
SDKKLPR
Catalog Number
SDKKLPR
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-02-14
Public Version
1
Public Version Date
2025-02-24
Public Version Status
New
Public Device Record Key
1dd8af43-50fa-4e1c-b5a0-2f3965be636f

Device Description

SDKKLP @RELIEVA SIDEKICK RELIEVA SINUS G

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KAM CANNULA, SINUS

GMDN Terms

Code Name
48142 Paranasal sinus guide-catheter

Identifiers

Type ID
Package 20080196392275
Primary 10080196392278

Customer Contacts