Medline Industries, Inc. DYNJ905172C

GUDID 10193489653618

FHWC ARTHROSCOPY

MEDLINE INDUSTRIES, INC.

General/plastic surgical procedure kit, non-medicated, single-use

• Primary Device ID: 10193489653618
• NIH Device Record Key: 066a989b-32f1-445d-a818-0129c7d9cdc4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Medline Industries, Inc.
• Version Model Number: DYNJ905172C
• Catalog Number: DYNJ905172C
• Company DUNS: 025460908
• Company Name: MEDLINE INDUSTRIES, INC.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)633-5463
• Email: customerservice@medline.com
• Phone: +1(800)633-5463
• Email: customerservice@medline.com
• Phone: +1(800)633-5463
• Email: customerservice@medline.com
• Phone: +1(800)633-5463
• Email: customerservice@medline.com
• Phone: +1(800)633-5463
• Email: customerservice@medline.com
• Phone: +1(800)633-5463
• Email: customerservice@medline.com
• Phone: +1(800)633-5463
• Email: customerservice@medline.com
• Phone: +1(800)633-5463
• Email: customerservice@medline.com
• Phone: +1(800)633-5463
• Email: customerservice@medline.com
• Phone: +1(800)633-5463
• Email: customerservice@medline.com
• Phone: +1(800)633-5463
• Email: customerservice@medline.com
• Phone: +1(800)633-5463
• Email: customerservice@medline.com
• Phone: +1(800)633-5463
• Email: customerservice@medline.com
• Phone: +1(800)633-5463
• Email: customerservice@medline.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10193489653618 [Primary]

FDA Product Code

• OJH: Orthopedic tray

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-04-01
• Device Publish Date: 2019-03-24

On-Brand Devices [Medline Industries, Inc.]

• 10889942912155: ANGIO PACK
• 10889942598878: KIT,CLN UP/ADBN ASC @ST FRANCS
• 10889942496198: ARTHROGRAM TRAY
• 10889942439805: MATHEWSON PACK
• 10193489654998: VAGINAL DELIVERY PACK-LF
• 10193489654813: SIH TOTAL SHOULDER
• 10193489654776: MHC MAJOR ABDOMINAL DRAPE
• 10193489654349: HHOR LITHOTOMY
• 10193489654233: TOTAL SHOULDER TRENHAILE
• 10193489654165: PODIATRY PACK
• 10193489654141: SUPPLEMENTAL CRANIOTOMY PK-LF
• 10193489654134: MINOR PK-LF
• 10193489654127: CATH LAB PACK-LF
• 10193489654042: NETWORK HAND PACK
• 10193489654035: VASCULAR-LF
• 10193489654004: ARTERIOGRAM PACK-LF
• 10193489653991: CORE BIOPSY PACK
• 10193489653977: MINOR PROCEDURE PACK-LF
• 10193489653946: LAPAROSCOPY CDS
• 10193489653830: NEURO
• 10193489653809: TOTAL SHOULDER
• 10193489653748: ORTHO SPINE
• 10193489653649: FHWC TOTAL KNEE
• 10193489653625: FHWC EXTREMITY PACK
• 10193489653618: FHWC ARTHROSCOPY
• 10193489653595: KNEE ARTHROSCOPY
• 10193489653588: NEURO/SPINE-LF
• 10193489653571: TAVI
• 10193489653410: TOTAL KNEE
• 10193489653403: GENERAL LAPAROSCOPY
• 10193489653311: TOTAL KNEE PACK
• 10193489653304: EAR PACK
• 10193489653298: ANGIOGRAPHY PACK
• 10193489653274: NETWORK CYSTO PACK-LF
• 10193489653243: TOTAL HIP
• 10193489653236: LAMINECTOMY
• 10193489653212: SPINAL SKOKIE
• 10193489653144: HIP PACK MAIN
• 10193489653120: TOTAL KNEE-LF
• 10193489652963: ARTHROSCOPY PACK
• 10193489652925: CATARACT PACK
• 10193489652918: CV-TABLE PT2 PACK
• 10193489652901: CV TABLE PACK
• 10193489652888: CRMC UNIVERSAL PACK-LF
• 10193489652819: ANESTHESIA CIRCUIT-LF
• 10193489652802: SINGLE SHOT EPIDURAL
• 10193489652796: SPINAL TRAY 27G X 3.5
• 10193489652789: PROCEDURAL TRAY
• 10193489652772: SUPPORT TRAY
• 10193489652758: MINOR PROCEDURE