Ti-MESH

Primary DI
04042301102775
Brand
Ti-MESH
Company
pfm medical titanium gmbh
Model
6000470
Device description
Ti-MESH 4" X 6" Strong 65g/m²
Published
2021-11-01
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

Contact Domains#

Product Codes#

Code, Name table
CodeName
FTLMesh, Surgical, Polymeric

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FTLMesh, Surgical, PolymericGeneral, Plastic Surgery2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K031225000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K031225000TIMESH ALSO KNOWN AS TIMESH-TC, MODELS 6000001 & 6000004Gfe Medizintechnik GmbH2003-09-29FTL

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
04042301102775PackageGS13In Commercial Distribution
04042301102768PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
04042301102775040423011027754042301102775
04042301102768040423011027684042301102768

GMDN Terms#

Term, Definition table
TermDefinition
Abdominal hernia surgical mesh, composite-polymerA flat or three-dimensional (3-D), woven/knitted material made of two or more polymers that includes a bioabsorbable polymer [e.g., polyglycolic acid (PGA)] and a non-bioabsorbable polymer [e.g., polyethylene (PE)] intended to be permanently implanted for abdominal hernia (e.g., inguinal, ventral/incisional, umbilical, femoral) and fascial defect repair/reinforcement applications; it is not intended for extra-abdominal applications and not dedicated to diaphragmatic hernia repair. It may also be used as a short-term scaffold for tissue regeneration. Disposable devices associated with implantation (e.g., introducer needles, trocars) may be included.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
7607588749regulatory@pfmmedicalusa.com

Regulatory Flags#

DUNS number
344675942
Device count
1
DM exempt
false
Premarket exempt
false
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
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
04042301097545TiMESH60001372019-12-09
04042301097569TiMESH60001382019-12-09
04042301097644TiMESH60001402019-12-09
04042301144317TiMESH60007372019-12-09
04042301144331TiMESH60007382019-12-09
04042301097668TiMESH60001392019-12-09
04042301097583Ti-MESH60003112021-11-01
04042301097620Ti-MESH60002482021-11-01
04042301102768Ti-MESH60004702021-11-01
04042301117397Ti-MESH60004712021-11-01
04042301117786Ti-MESH60004232021-11-01
04042301117809Ti-MESH60004242021-11-01
04042301097606TiMESH60003122020-06-02
04042301097590Ti-MESH60003112021-11-01
04042301097637Ti-MESH60002482021-11-01
04042301137173Ti-MESH60004712021-11-01
04042301117793Ti-MESH60004232021-11-01
04042301097552TiMESH60001372019-12-09
04042301097576TiMESH60001382019-12-09
04042301097651TiMESH60001402019-12-09

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09421906661569OviTex® LPRAROA BIOSURGERY LIMITEDFTL2023-06-15
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