Treatment Pack (Size M)

Primary DI
04049471110142
Brand
Treatment Pack (Size M)
Company
Carl Zeiss Meditec AG
Model
1014
Device description
single use accessory for ZEISS femtosecond lasers
Published
2024-02-09
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
HNOKeratome, Ac-Powered
HQFLaser, Ophthalmic
OTLFemtosecond Laser System For Refractive Correction

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HNOKeratome, Ac-PoweredOphthalmic1
HQFLaser, OphthalmicOphthalmic2
OTLFemtosecond Laser System For Refractive CorrectionUnknown3

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
P150040012

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
P150040012VISUMAX FEMTOSECOND LASERCarl Zeiss Meditec, Inc.2016-09-13OTL

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
04049471110142PrimaryGS10
04049471100143Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
04049471110142040494711101424049471110142
04049471100143040494711001434049471100143

GMDN Terms#

Term, Definition table
TermDefinition
Femtosecond ophthalmic solid-state laser systemA mains electricity (AC-powered) device assembly in which input energy (e.g., flashlamp, diode laser) is used to excite a glass/crystal rod to emit a high-power laser beam intended for ocular resections and incisions (cataract incisions, arcuate corneal/scleral cuts/tunnels, anterior capsulotomy, phacofragmentations, corneal flaps, lamellar/perforating keratoplasty). The system includes a beam delivery device, imaging device, computer, software and controls; it cuts by micro-photodisruption of tissue created by focused ultra-short [femtosecond (FS)] pulses; it does not include fundus imaging technology and the therapeutic laser is not frequency-doubled.

Regulatory Flags#

DUNS number
314594680
Device count
10
Lot or batch
true
Manufacturing date on label
true
Expiration date on label
true

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Primary DI, Brand, Model table
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04049471090260AT 030AT 0302018-12-04
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04049539105547INTRABEAM SMART Spherical Applicator (35 mm)309120-9035-0002025-05-14
04049539105554INTRABEAM SMART Spherical Applicator (35mm)309120-9035-0002025-05-14
04049539105561INTRABEAM SMART Spherical Applicator (40mm)309120-9040-0002025-05-14
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04049539101570INTRABEAM® Spherical Applicator 2.0 cm304534-6000-5582017-04-14
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Primary DI, Brand, Company table
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