Sentrex BioSponge MPD

Primary DI
00850047730107
Brand
Sentrex BioSponge MPD
Company
Bionova Medical Inc.
Model
501-1020
Published
2023-09-24
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
FRODressing, Wound, Drug

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FRODressing, Wound, DrugUnknownU

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K123961000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K123961000SENTREX BIOSPONGE MPDBionova Medical, Inc.2013-04-05KGN

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00850047730107PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00850047730107008500477301078500477301070850047730107

GMDN Terms#

Term, Definition table
TermDefinition
Cavity-wound management dressing, non-antimicrobialA non-bioabsorbable material or substance designed to be inserted into a wound bed to create an appropriate environment for healing (e.g., warm, moist, absorbent); it does not include an antimicrobial agent(s). It is typically used for the management of deep secondary-healing wounds, particularly for indications such as stage III and IV pressure ulcers, deep leg ulcers, cavity wounds, excisions, and post-op wound dehiscence. It is often designed to conform to the wound bed to support tissues and is often nonadherent to provide for patient comfort during wound management. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Length10Centimeter
Width20Centimeter

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
901-748-2581info@bionovamedical.com

Regulatory Flags#

DUNS number
080325588
Device count
1
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00850047730305Foundation DRS SoloFS1-00032025-09-17
00850047730312Foundation DRS SoloFS1-00092025-09-17
00850047730329Foundation DRS SoloFS1-02032025-09-17
00850047730336Foundation DRS SoloFS1-04042025-09-17
00850047730343Foundation DRS SoloFS1-202522025-09-17
00850047730008Foundation DRS SoloFS1-05052023-07-05
00850047730015Foundation DRS SoloFS1-10122023-07-05
00850047730022Foundation DRS SoloFS1-10252023-07-05
00850047730039Foundation DRS SoloFS1-20252023-07-05
00850047730046Foundation DRS SoloFS1-F-05052023-07-05
00850047730053Foundation DRS SoloFS1-F-10122023-07-05
00850047730060Foundation DRS SoloFS1-F-10252023-07-05
00850047730077Foundation DRS SoloFS1-F-20252023-07-05
00850047730114Foundation DRS+ Duo802-05052024-08-26
00850047730121Foundation DRS+ Duo802-10122024-08-26
00850047730138Foundation DRS+ Duo802-10252024-08-26
00850047730145Foundation DRS+ Duo802-20252024-08-26
00850047730152Foundation DRS+ Duo902-05052024-08-26
00850047730169Foundation DRS+ Duo902-10122024-08-26
00850047730176Foundation DRS+ Duo902-10252024-08-26

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