FDA.reportPublic FDA data

CS 7600 Hygienic Sheath

Primary DI
60889971014382
Brand
CS 7600 Hygienic Sheath
Company
CARESTREAM HEALTH, INC.
Model
CS 7600 Hygienic Sheath
Catalog number
1014380
Device description
CS 7600 HYG SHEATHS SIZE 2 200 PCS
Published
2016-09-16
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
false
Single use
true

Product Codes#

Code, Name table
CodeName
KQMCAMERA, SURGICAL AND ACCESSORIES

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KQMCamera, Surgical And AccessoriesGeneral, Plastic Surgery1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
60889971014382PackageGS120In Commercial Distribution
40889971014388PrimaryGS10
00889971014380Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
6088997101438260889971014382
4088997101438840889971014388
00889971014380008899710143808899710143800889971014380

GMDN Terms#

Term, Definition table
TermDefinition
Cable/lead/sensor/probe cover, sterileA sterile device, typically made of disposable plastic, that forms a protective enclosure around its cable/lead, probe, sensor, or tube contents, making a hygienic barrier so that the non-sterile contents may enter a hygienic area, e.g., a sterile surgical field. This is a single-use device.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Storage Environment Temperature10 Degrees Celsius24 Degrees Celsius

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
793169512
Device count
200
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
60889976701171CARESTREAM Image SuiteCARESTREAM Image Suite67011712022-02-25
60889971001894Vue Cardio PACSVue Cardio PACS10018902016-09-16
60889971029881DRX - Ascend SystemDRX - Ascend System10298832017-07-24
60889971041692Vue PACSVue PACS12012842016-09-16
60889971047809Vue PACSVue PACS11494182016-09-16
60889971048875Vue MotionVue Motion10179792016-09-16
60889971055989CARESTREAM Image SuiteCARESTREAM Image Suite10559872016-09-16
60889978624188DRX-Compass X-ray SystemDRX-Compass X-ray System86241812022-01-11
60889971739193DRX-Evolution Plus SystemDRX-Evolution Plus System17391922016-09-16
60889978007257DRX-Revolution Mobile X-ray SystemDRX-Revolution Mobile X-ray System80072542016-09-16
60889976565667CARESTREAM DRX-EVOLUTIONCARESTREAM DRX-EVOLUTION65656672016-09-16
40889971067506CS 7200CS 720010675032016-09-16
40889971067513CS 7200CS 720010675112016-09-16
40889971337227CS 7400CS 740013372292016-09-16
40889978214231CS 7400CS 740082142312016-09-16
40889978427969CS 7400CS 740084279652016-09-16
40889978666948CS 7400CS 740086669432016-09-16
60889976579336Vita Flex CR SystemVita Flex CR System65793382019-08-03
60889976579343Vita Flex CR SystemVita Flex CR System65793462019-08-03
60889976579367Vita Flex CR SystemVita Flex CR System65793612019-08-03

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00819761023063Optik ViewLINDEN GROUP CORPORATION, THEKQM2026-06-05
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00819761023094Optik ViewLINDEN GROUP CORPORATION, THEKQM2026-06-04
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14714127861392AESCULAPAesculap AGKQM2023-11-05
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