Geistlich Mucograft® Seal

Primary DI
07610221011308
Brand
Geistlich Mucograft® Seal
Company
Geistlich Pharma AG
Model
50-0808
Published
2015-09-01
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
NPLBarrier, Animal Source, Intraoral

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
NPLBarrier, Animal Source, IntraoralDental2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K140518000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K140518000GEISTLICH MUCOGRAFT: 15 X 20 MM, 20 X 30 MM, 8 MM DIAMETERGeistlich Pharma AG2014-07-18NPL

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
07610221011308PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
07610221011308076102210113087610221011308

GMDN Terms#

Term, Definition table
TermDefinition
Dental soft-tissue matrix implant, animal-derivedA sterile bioabsorbable material intended to be used to aid in the regeneration of oral soft tissue, lost due to periodontal disease or trauma, primarily through promotion of new blood vessels; it is indicated for various oral soft tissue augmentation procedures (e.g. alveolar ridge reconstruction, localized gingival augmentation, covering of recession defects and extraction sockets). It is a pliable material made of animal-derived collagen (e.g., porcine) which may be fixed to soft tissues with sutures; it is applied to soft tissue by properly prepared flaps during periodontal flap surgery and guided tissue regeneration (GTR) surgical procedures. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Outer Diameter8Millimeter

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
480781728
Device count
1
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
07610221017737Derma-Gide®5020102026-06-01
07610221017829Device 300423 Granules5021902026-06-01
07610221017836Device 300423 Granules5021912026-06-01
07610221017843Device 300423 Granules5021922026-06-01
07610221017850Device 300423 Granules5021932026-06-01
07610221017867Device 300423 Granules5021942026-06-01
07610221017874Device 300423 Granules5021952026-06-01
07610221017881Device 300423 Granules5021962026-06-01
07610221017898Device 300423 Granules5021972026-06-01
07610221017904Device 300423 Granules5021982026-06-01
07610221017911Device 300423 Granules5021992026-06-01
07610221017928Device 300423 Granules5022002026-06-01
07610221017645Bionnovation Gide XP5021702026-05-08
07610221017652Bionnovation Gide XP5021712026-05-08
07610221017669Bionnovation Gide XP5021722026-05-08
07610221017201Geistlich Bio-Gide®5021132026-04-09
07610221017126Derma-Gide®5004272025-07-01
07610221017133Derma-Gide®5004742025-07-01
07610221017140Derma-Gide®5004802025-07-01
07610221015481Geistlich Fibro-Gide®5008382022-09-09

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