n.a.

Primary DI
04048551260128
Brand
n.a.
Company
Karl Storz GmbH & Co. KG
Model
11101CM
Device description
CMOS Video-Rhino-Laryngoscope
Published
2016-09-23
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true

Product Codes#

Code, Name table
CodeName
EOBNASOPHARYNGOSCOPE (FLEXIBLE OR RIGID)

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
EOBNasopharyngoscope (Flexible Or Rigid)Ear, Nose, Throat2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K103467000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K103467000CMOS VIDEO RHINO-LARYNGOSCOPE SYSTEM MODEL 11101CMKARL STORZ Endoscopy-America, Inc.2012-06-28EOB

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
04048551260128PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
04048551260128040485512601284048551260128

GMDN Terms#

Term, Definition table
TermDefinition
Flexible video otorhinolaryngoscope, reusableAn endoscope with a flexible inserted portion intended for the visual examination of some or all of the ear (external, middle and inner), nasal passages, paranasal sinuses, pharynx, and/or larynx. It is inserted into the body through the appropriate natural orifice and can be used for treatment if it has a working channel. Anatomical images are transmitted to the user by a video system with an image sensor chip at the distal end of the endoscope and the images showing on a monitor (not included); it may include an irrigation/suction channel. This is a reusable device.

Sterilization Methods#

Method table
Method
"[""Liquid Chemical"", ""Peracetic Acid"", ""Ethylene Oxide"", ""Hydrogen Peroxide""]"
Liquid Chemical;Peracetic Acid;Ethylene Oxide;Hydrogen Peroxide

Regulatory Flags#

DUNS number
315731430
Device count
1
Serial number
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
04048551161005n.a.408001102018-09-04
04048551291030NAV1408100202018-08-23
04048551325971n.a.408000212016-09-23
04048551160992n.a.408000902016-09-23
04048551277577n.a.408120202018-08-21
04048551325988n.a.408000512016-09-23
04048551336854NAV1408200202018-08-23
04048551337707n.a.408200862018-08-17
04048551337820NAV1408200302018-08-23
04048551271087n.a.408001202016-09-23
04048551387344n.a.408201232019-02-23
04048551387368n.a.408201502017-03-17
04048551001141n.a.495NCS2016-09-23
04048551004401n.a.495TIP2016-09-23
04048551004463n.a.50200FFL2018-08-21
04048551028568n.a.495ADM2016-09-23
04048551049549n.a.10970AE2018-08-17
04048551049563n.a.10970BE2018-08-17
04048551052495n.a.12016EM2016-09-23
04048551052525n.a.12016FM2016-09-23

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Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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04580826921117PENTAX MedicalPENTAX MEDICAL CORPORATIONEOB2026-08-25
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04580826925948VIVIDEOPENTAX MEDICAL CORPORATIONEOB2026-08-25
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04580826926006VIVIDEOPENTAX MEDICAL CORPORATIONEOB2026-08-25
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