MULTI-GUIDE

Primary DI
04546540257673
Brand
MULTI-GUIDE
Company
Stryker Leibinger GmbH & Co. KG
Model
62-01000
Catalog number
62-01000
Device description
MANDIBULAR DISTRACTION DEVICE
Published
2015-09-24
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Single use
true

Product Codes#

Code, Name table
CodeName
MQNEXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
MQNExternal Mandibular Fixator And/Or DistractorDental2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K960297000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K960297000MANDIBULAR BONE DISTRACTOR IIHowmedica Corp.1996-08-06MQN

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
04546540257673PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
04546540257673045465402576734546540257673

GMDN Terms#

Term, Definition table
TermDefinition
Implantable craniofacial bone distractorAn implantable or partially-implantable device intended to temporarily distract (force apart) the two bone surfaces of the mandible (the lower jawbone) or maxilla (the upper jawbone) during craniomaxillofacial (CMF) distraction. It functions as a single-patient bone lengthening/augmentation device for the correction of congenital deficiencies or post-traumatic defects when gradual bone augmentation is required. It typically consists of a metal tube in which a right- and left-hand threaded rod rotates and to which are attached two craniofacial fixation plates that are surgically screwed to either side of the fracture. A small tip guard may be included to protect against inadvertent rotation.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Length20Millimeter

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
316153956
Device count
1
Lot or batch
true
Manufacturing date on label
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
07613327300086NA78-8002078-800202021-01-27
07613327300109NA78-8004078-800402021-01-27
07613327300123NA78-8003078-800302021-01-27
04546540730763NA78-1001078-100102015-07-03
04546540730787NA78-1003078-100302015-07-03
04546540730794NA78-1004078-100402015-07-03
04546540730800NA78-1010078-101002015-07-03
07613327004021NA78-1002078-100202015-07-03
07613327129236NA78-4001078-400102015-09-24
07613327129243NA78-4010078-401002015-09-24
07613327129250NA78-4004078-400402015-09-24
07613327129267NA78-5003078-500302015-09-24
07613327129274NA78-5004078-500402015-09-24
07613327129281NA78-5002078-500202015-09-24
07613327129298NA78-4003078-400302015-09-24
07613327129328NA78-5001078-500102015-09-24
07613327129335NA78-4002078-400202015-09-24
07613327300017NA78-7002078-700202017-02-21
07613327300031NA78-7004078-700402017-02-21
07613327300055NA78-7003078-700302017-02-21

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Primary DI, Brand, Company table
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