Braun

Primary DI
10328785000525
Brand
Braun
Company
KAZ, INC.
Model
PRO6000RBV1
Device description
Battery, Replacement, PRO6000 Series
Published
2018-04-30
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
true
Sterile
false
Single use
false

Contact Domains#

Product Codes#

Code, Name table
CodeName
FLLThermometer, Electronic, Clinical

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FLLContinuous Measurement ThermometerGeneral Hospital2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K152748000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K152748000Braun Thermoscan PRO 6000 Ear ThermometerKaz USA, Inc (A Subsidiary of Helen of Troy, Inc)2016-03-01FLL

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10328785000525PackageGS125In Commercial Distribution
00328785000528PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1032878500052510328785000525
00328785000528003287850005283287850005280328785000528

GMDN Terms#

Term, Definition table
TermDefinition
Rechargeable battery packA group of rechargeable batteries held within a holder or container intended to provide temporary electrical energy to operate a medical device, typically when it is not possible, intentional, or convenient to connect the device being powered to a mains electricity (AC-powered) electrical outlet. It is typically used during a transport situation (e.g., a neonatal incubator), or when the device is designed to power a cordless devices (e.g., an endoscopic device or a rechargeable battery-powered surgical drilling system handpiece). This is a reusable device.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
1-800-477-0457consumerrelations@kaz.com

Regulatory Flags#

DUNS number
001483890
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
false
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#

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10328785002352HONEYWELLHUL900B2021-09-30
10328785002468Vicks VUL9002021-09-30
00328785002034VicksVNT200US2020-09-29
20328785002038VicksVNT200US2020-09-29
10328785004820VicksV4600V22020-04-03
10328785004837HoneywellHUL535WV22020-04-03
10328785004844HoneywellHUL535BV22020-04-03
10328785004875HoneywellHUL520LV32020-04-03
10328785004882HoneywellHUL520RV32020-04-03
10328785004868HoneywellHUL520BV32020-01-28
10328785003212VicksVUL6002019-12-30

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