FDA.reportPublic FDA data

Medline Industries, Inc.

Primary DI
10888277921696
Brand
Medline Industries, Inc.
Company
MEDLINE INDUSTRIES, INC.
Model
ACC010276A
Catalog number
ACC010276A
Device description
439791 IV ACCESS/SYR & NEEDLE
Published
2016-09-28
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
FPASet, administration, intravascular

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FPASet, Administration, IntravascularGeneral Hospital2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K003225000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K003225000SOLUTION ADMINISTRATION SETS WITH CAPLESS LUER ACTIVATED VALVEBaxter Healthcare Corp2000-10-19FPA

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10888277921696PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized table
Source identifierGTIN-14 normalized
1088827792169610888277921696

GMDN Terms#

Term, Definition table
TermDefinition
General surgical procedure kit, non-medicated, reusableA typically non-dedicated collection of various surgical instruments, sometimes with dressings and/or other materials, but that does not contain pharmaceuticals, intended to be used during: 1) open abdominal surgery; 2) a range of open surgical procedures across multiple clinical specialties (non-dedicated); 3) non-orthopaedic trauma surgery; 4) minor dermatological surgery; or 5) cosmetic surgery below the head. As a kit that includes procedural devices, it is neither dedicated to surgical scrubbing, surgical patient preparation, nor anaesthesia, and is not a dedicated biopsy kit. This is a reusable device.

Contacts#

Phone, Email table
PhoneEmail
+1(800)633-5463customerservice@medline.com

Regulatory Flags#

DUNS number
025460908
Device count
1
DM exempt
true
Kit
true
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
10197344039791MEDLINEHNX22075HNX220752024-10-11
10197344039807MEDLINEHNX22100HNX221002024-10-11
10888277348226MEDLINEMDS630S2MDS630S22026-07-29
10888277699472MEDLINEDYND300010SDYND300010S2026-07-29
10888277699489MEDLINEDYND300015SDYND300015S2026-07-29
10888277699496MEDLINEDYND300020SDYND300020S2026-07-29
10888277699502MEDLINEDYND300025SDYND300025S2026-07-29
10888277699533MEDLINEDYND300050SDYND300050S2026-07-29
10888277701588MEDLINEMSC9912EPMSC9912EP2025-09-24
10888277701595MEDLINEMSC9918EPMSC9918EP2025-09-24
10888277701618MEDLINEMSC9945EPMSC9945EP2025-09-24
10888277701625MEDLINEMSC9948EPMSC9948EP2025-09-24
10888277701632MEDLINEMSC9966EPMSC9966EP2025-09-24
10888277701649MEDLINEMSC99812EPMSC99812EP2025-09-24
30193489103964MEDLINE1202YLW3AOS2026-07-28
30193489103971MEDLINE1202YLW3XL2026-07-28
10197344216123MEDLINESSBCS21GLSSBCS21GL2026-07-24
10197344219575MEDLINEMDS99905MDS999052026-07-24
10653160391326MEDLINEEBSI1865EBSI18652026-07-24
30193489017742MEDLINE6651CBL22X16651CBL22X12026-07-24

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