FDA.reportPublic FDA data

URGOK2 LITE

Primary DI
03546890028450
Brand
URGOK2 LITE
Company
LABORATOIRES URGO
Model
553246
Device description
A 2-layer reduced multicomponent compression bandage system, composed of a short stretch bandage and a long stretch bandage.Layer 1, KTECH Lite/KTECH Reduced composition: wadding: viscose, polyester; knitted layer: polyamide, elastane.Layer 2, KPRESS composition: cotton, polyester, polyamide, elastane; synthetic latex free cohesive material.
Published
2021-04-26
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
FQMBandage, Elastic

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FQMBandage, ElasticGeneral Hospital1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
03546890028450PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
03546890028450035468900284503546890028450

GMDN Terms#

Term, Definition table
TermDefinition
Compression bandaging kitA collection of various types of non-sterile bandages intended for use in the treatment of venous leg ulcers, and related conditions, by sequential bandage application to provide graduated ascending-decreasing compression from the ankle to the knee. Typically the bandages are applied in a sequence of layers: a padding/exudate absorbing layer (e.g., polyester), a retention layer (e.g., cotton/polyester/elastane), a compression (e.g., viscose/polyester covered elastane) and a self-adherent compression/outer retention layer (e.g., latex/polyester/elastane). It is intended to be applied by a healthcare professional for use in the home or healthcare facility. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Special Storage Condition, Specify00Keep away from sunlight
Special Storage Condition, Specify00Store away from light

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
855-888-8273info@us.urgo.com

Regulatory Flags#

DUNS number
397310355
Device count
1
Premarket exempt
true
Kit
true
Lot or batch
true
Expiration date on label
true
No natural rubber latex
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
03546890046379URGOCLEAN AG PAD6040382026-04-14
03546890046461URGOCLEAN AG PAD6040602026-04-14
03546890046782URGOCLEAN AG PAD6041242026-04-14
03546890044290URGOTUL ABSORB BORDER6035532024-11-19
03546890043286URGOTUL6042302025-11-03
03546890047840URGOTUL6043662025-11-03
03546890047932URGOTUL6042982025-11-03
03546890048083URGOTUL6043722025-11-03
03546890048205URGOTUL6043622025-11-03
03546890043255URGOTUL ABSORB6036392024-11-19
03546890043507URGOTUL ABSORB BORDER6035622024-11-19
03546890044016URGOTUL ABSORB BORDER6035172024-11-19
03546890044443URGOTUL ABSORB BORDER6035752024-11-19
03546890044955URGOTUL ABSORB6036342024-11-19
03546890045174URGOTUL ABSORB6036502024-11-19
03546890045297URGOTUL ABSORB6036622024-11-19
03546890045044URGOTUL ABSORB6036392024-11-19
03546890044405URGOTUL ABSORB BORDER6035622024-11-19
03546890044009URGOTUL ABSORB BORDER6035172024-11-19
03546890044177URGOTUL ABSORB BORDER6035532024-11-19

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