FDA.reportPublic FDA data

V. Mueller

Primary DI
00724995270957
Brand
V. Mueller
Company
STERIS Deutschland GmbH
Model
AU12080
Catalog number
AU12080
Device description
V. Mueller ROSEN PROBE OVERALL LENGTH 6-1/4 inches 16 CM
Published
2026-09-25
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Contact Domains#

Product Codes#

Code, Name table
CodeName
KAKPROBE, ENT

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KAKProbe, EntEar, Nose, Throat1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10885403009624PreviousGS10
00724995270957PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1088540300962410885403009624
00724995270957007249952709577249952709570724995270957

GMDN Terms#

Term, Definition table
TermDefinition
Abdominal/ENT/orthopaedic surgical probe, reusableA slender, rod-like, hand-held manual surgical instrument intended to be used to explore cavities, wounds or fistulas during abdominal, ENT, and/or orthopaedic surgical interventions; it does not include stereotactic devices and is not dedicated to endoscopy. It may have a blunt bulbous, paddle-like, or pointed tip, may be single- or double-ended, and the shaft may be straight, bent or hooked. It is made of rigid or flexible metallic and/or synthetic polymer material. This is a reusable device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1(800)548-4873xx@xx.xx

Regulatory Flags#

DUNS number
537625100
Device count
1
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
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00724995267742Snowden-Pencer8820108820102026-09-25
00724995267773Snowden-Pencer8821118821112026-09-25
00724995267780Snowden-Pencer8821238821232026-09-25
00724995267797Snowden-Pencer8821248821242026-09-25
00724995267803Snowden-Pencer8821288821282026-09-25
00724995267896Snowden-Pencer8824008824002026-09-25
00724995267902Snowden-Pencer8830108830102026-09-25
00724995267926Snowden-Pencer8830508830502026-09-25
00724995267940Snowden-Pencer8832008832002026-09-25
00724995267957Snowden-Pencer8832018832012026-09-25
00724995267995Snowden-Pencer8838628838622026-09-25
00724995268008Snowden-Pencer8838678838672026-09-25
00724995268015Snowden-Pencer8838738838732026-09-25
00724995268022Snowden-Pencer8838758838752026-09-25
00724995268039Snowden-Pencer8838768838762026-09-25
00724995268046Snowden-Pencer8838788838782026-09-25
00724995268312Snowden-Pencer8850508850502026-09-25
00724995268329Snowden-Pencer8850518850512026-09-25
00724995268336Snowden-Pencer8850528850522026-09-25
00724995268343Snowden-Pencer8850538850532026-09-25

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
04054462915071evonosevonos GmbH & Co. KGKAK2026-08-25
04054462915088evonosevonos GmbH & Co. KGKAK2026-08-25
04054462915095evonosevonos GmbH & Co. KGKAK2026-08-25
04054462915101evonosevonos GmbH & Co. KGKAK2026-08-25
04054462905751evonosevonos GmbH & Co. KGKAK2026-08-21
04054462901203evonosevonos GmbH & Co. KGKAK2026-08-18
00840183532963BR Surgical, LLCBR Surgical, LLCKAK2026-07-17
00840183532970BR Surgical, LLCBR Surgical, LLCKAK2026-07-17
00850083275990Intrace USAPILOTIS TECH LLCKAK2026-07-03
09348811115829INKAThe Trustee for KAISER FAMILY TRUSTKAK2026-04-24
09348811005106INKAThe Trustee for KAISER FAMILY TRUSTKAK2026-03-18
00714646001535Lighted Magnetic Foreign Body Removal ToolBionix, LLCKAK2026-03-03
10714646001532Lighted Magnetic Foreign Body Removal ToolBionix, LLCKAK2026-03-03
00714646001627Lighted Magnetic Foreign Body Removal ToolBionix, LLCKAK2026-03-03
09348811115836INKAThe Trustee for KAISER FAMILY TRUSTKAK2025-11-25
09348811112149INKAThe Trustee for KAISER FAMILY TRUSTKAK2025-11-21
09348811150448INKAThe Trustee for KAISER FAMILY TRUSTKAK2025-11-21
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04250676740632Bowman salivary duct probeSpiggle & Theis Medizintechnik GmbHKAK2025-09-29
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04250676740663Bowman salivary duct probeSpiggle & Theis Medizintechnik GmbHKAK2025-09-29
04250676740687Bowman salivary duct probeSpiggle & Theis Medizintechnik GmbHKAK2025-09-29
04250676740694Bowman salivary duct probeSpiggle & Theis Medizintechnik GmbHKAK2025-09-29