FDA.report

MEDLINE

Primary DI
20193489194897
Brand
MEDLINE
Company
MEDLINE INDUSTRIES, INC.
Model
DYNDV2335
Catalog number
DYNDV2335
Device description
SUREVIEW 2X3IN STRL DRESSING
Published
2020-04-23
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Related Records

Contact Domains

Product Codes

CodeName
KMKDEVICE, INTRAVASCULAR CATHETER SECUREMENT

Product Code Classifications

CodeDeviceSpecialtyClass
KMKDevice, Intravascular Catheter SecurementGeneral Hospital1

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
20193489194897PackageGS120In Commercial Distribution
10193489194890PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalized
2019348919489720193489194897
1019348919489010193489194890

GMDN Terms

TermDefinition
Wearable percutaneous catheter/tube holderA device designed to fix a percutaneous catheter, tube, and/or drain (e.g., IV, epidural, or drainage catheter, GI tube) to a patient's body without suturing; it may additionally be intended for holding a non-surgically-invasive tube (e.g., nasogastric tube) to the patient (universal holder). It is designed as an adhesive pad, strip, or bandage that will attach to the patient's skin, sometimes with the exposed side having an integrated fixation mechanism (e.g., Velcro hook/loop closure) or a mechanical closure, to hold the catheter/tube in place. It may include a transparent film portion intended for fixation site monitoring. This is a single-use device.

Sterilization Methods

Method

Contacts

PhoneEmail
+1(800)633-5463CUSTOMERSERVICE@MEDLINE.COM

Regulatory Flags

DUNS number
025460908
Device count
1
DM exempt
true
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
true
Sterilization required before use
false

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10080196258598MEDLINEMDT013020457MDT0130204572016-10-14
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10080196363773MEDLINEMDT013667MDT0136672016-10-14
10080196363803MEDLINEMDT013673FMDT013673F2016-10-14
10197344039746MEDLINEHNX19100HNX191002024-10-11
10197344039784MEDLINEHNX20150HNX201502024-10-11
10197344039838MEDLINEHNY19100HNY191002024-10-11
10197344039845MEDLINEHNY19150HNY191502024-10-11
10197344039852MEDLINEHNY20075HNY200752024-10-11
10197344039869MEDLINEHNY20100HNY201002024-10-11
10197344039876MEDLINEHNY20150HNY201502024-10-11
10197344039883MEDLINEHNY22075HNY220752024-10-11
10197344039890MEDLINEHNY22100HNY221002024-10-11
10197344039906MEDLINEHNY22150HNY221502024-09-27
10197344099771MEDLINEAVT0665AVT06652025-03-10

Other Devices Sharing Product Codes

Primary DIBrandCompanyProduct codePublished
05430004283935FlexGRIPBedalKMK2025-12-19
05430000258494FlexGRIPBedalKMK2025-12-03
05430000258654Bedal BedalKMK2025-12-03
05430003674017FlexGRIPBedalKMK2025-12-03
05430003674062FlexGRIPBedalKMK2025-12-03
05430003674239Bedal BedalKMK2025-12-03
05430003674260Bedal BedalKMK2025-12-03
05430004283812Bedal BedalKMK2025-12-03
05430003674116FlexGRIPBedalKMK2025-12-02
05430003674147FlexGRIPBedalKMK2025-12-02
05430003674321FlexGRIPBedalKMK2025-12-02
05430003674468FlexGRIPBedalKMK2025-12-02
05430003674499FlexGRIPBedalKMK2025-12-02
05430003674956FlexGRIPBedalKMK2025-12-02
05430003674987FlexGRIPBedalKMK2025-12-02
05430004283270FlexGRIPBedalKMK2025-12-02
05430004283355FlexGRIPBedalKMK2025-12-02
05430004283386FlexGRIPBedalKMK2025-12-02
05430004283416FlexGRIPBedalKMK2025-12-02
05430004283447FlexGRIPBedalKMK2025-12-02
05430004283478FlexGRIPBedalKMK2025-12-02
05430004283553FlexGRIPBedalKMK2025-12-02
05430004283584FlexGRIPBedalKMK2025-12-02
05430004283737FlexGRIPBedalKMK2025-12-02
05430004283768FlexGRIPBedalKMK2025-12-02
05430004283867FlexGRIPBedalKMK2025-12-02
05430000258173Bedal BedalKMK2025-12-01
05430000258258FlexGRIPBedalKMK2025-12-01
05430003674178FlexGRIPBedalKMK2025-12-01
05430003674208FlexGRIPBedalKMK2025-12-01