FDA.reportPublic FDA data

Procedure Pack

Primary DI
07640167750092
Brand
Procedure Pack
Company
SIE AG, Surgical Instrument Engineering
Model
10/100
Catalog number
510.701.140
Device description
Procedure Pack 10.0 mm, 100um flap Thickness
Published
2018-09-14
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

Contact Domains#

Product Codes#

Code, Name table
CodeName
GEXPowered Laser Surgical Instrument
HNOKeratome, Ac-Powered
HQFLaser, Ophthalmic

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GEXPowered Laser Surgical InstrumentGeneral, Plastic Surgery2
HNOKeratome, Ac-PoweredOphthalmic1
HQFLaser, OphthalmicOphthalmic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K053511000
K112154000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K053511000DA VINCI FEMTOSECOND SURGICAL LASERSie Ltd Surgical Instrument Engineering2006-03-10GEX
K112154000FEMTO LDVSie Ag,Surgical Instument Engineering2012-03-16HQF

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
07640167750634PackageGS110In Commercial Distribution
07640167750092PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
07640167750634076401677506347640167750634
07640167750092076401677500927640167750092

GMDN Terms#

Term, Definition table
TermDefinition
Ophthalmic surgical procedure kit, non-medicated, single-useA collection of various ophthalmic surgical instruments and the necessary materials intended to be used to perform an ophthalmic surgical procedure; it is not comprised exclusively of dedicated implantation tools and it does not contain any pharmaceuticals. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Height100Micrometer
Lumen/Inner Diameter10Millimeter

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Special Storage Condition, Specify00device kept at room / standard conditions

Contacts#

Phone, Email table
PhoneEmail
8667084490usa@ziemergroup.com

Regulatory Flags#

DUNS number
482163628
Device count
1
Kit
true
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
07640167750023FEMTO LDVZ6510.003.0062016-09-15
07640167750030FEMTO LDVZ4510.003.0042016-09-15
07640167750047FEMTO LDVZ2510.003.0022016-09-15
07640167750573FEMTOZ8 NEO510.003.0092022-06-10
07640167751334Procedure Pack Z8Cataract L2510.700.1192020-12-22
07640167751341Procedure Pack Z88.5 CS Z8 S510.700.1202020-12-22
07640167751358Procedure Pack Z89.0 CS Z8 S510.700.1212020-12-22
07640167751365Procedure Pack Z89.5 CS Z8 S510.700.1222020-12-22
07640167751372Procedure Pack Z810.0 CS Z8 S510.700.1232020-12-22
07640167751389Procedure Pack Z8L2510.700.1242020-12-22
07640167750108Procedure Pack10/110510.701.1412018-09-14
07640167750115Procedure Pack10/140510.701.1442018-09-14
07640167750122Procedure Pack10/90510.701.1492018-09-14
07640167750139Procedure Pack8.5/100510.701.1102018-09-14
07640167750146Procedure Pack8.5/110510.701.1112018-09-14
07640167750153Procedure Pack8.5/140510.701.1142018-09-14
07640167750160Procedure Pack8.5/90510.701.1192018-09-14
07640167750177Procedure Pack9.0/100510.701.1202018-09-14
07640167750184Procedure Pack9.0/110510.701.1212018-09-14
07640167750191Procedure Pack9.0/140510.701.1242018-09-14

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