FDA.reportPublic FDA data

V. Mueller

Primary DI
00724995270759
Brand
V. Mueller
Company
STERIS Deutschland GmbH
Model
AU11170
Catalog number
AU11170
Device description
V. Mueller LEMPERT HEAVY ELEVATOR BLADE 5MM WIDE OVERALL LENGTH 7-3/8 inches 18.7CM
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
KADELEVATOR, ENT

Product Code Classifications#

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

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10885403009341PreviousGS10
00724995270759PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1088540300934110885403009341
00724995270759007249952707597249952707590724995270759

GMDN Terms#

Term, Definition table
TermDefinition
ENT elevatorA hand-held, manually-operated, surgical instrument used to lift, position or pry anatomical structures or surgical material during ear/nose/throat (ENT) surgery. It may be a single or a double-ended device with a blunted blade or hook of various shapes with no cutting edges at the distal working end(s) and a handle positioned centrally or at the proximal end. Its shape and size depends upon the intended use, e.g., a blunt antrum, a rhinology or septum elevator, a strong nasal fracture elevator, or a specially designed ear elevator. It is usually made of high-grade stainless steel. 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
00724995266936Snowden-Pencer8810258810252026-10-15
00724995267391Snowden-Pencer8814258814252026-10-15
00724995267407Snowden-Pencer8814268814262026-10-15
00724995267414Snowden-Pencer8814278814272026-10-15
00724995267421Snowden-Pencer8814308814302026-10-15
00724995267445Snowden-Pencer8814328814322026-10-15
00724995267452Snowden-Pencer8814358814352026-10-15
00724995267469Snowden-Pencer8814418814412026-10-15
00724995267476Snowden-Pencer8814428814422026-10-15
00724995267933Snowden-Pencer8831038831032026-10-15
00724995268053Snowden-Pencer8838908838902026-10-15
00724995268060Snowden-Pencer8838918838912026-10-15
00724995268190Snowden-Pencer8840328840322026-10-15
00724995268206Snowden-Pencer8840338840332026-10-15
00724995268213Snowden-Pencer8840348840342026-10-15
00724995268220Snowden-Pencer8840358840352026-10-15
00724995317607V. MuellerOP190OP1902026-10-15
00724995317638V. MuellerOP191OP1912026-10-15
00724995317645V. MuellerOP192OP1922026-10-15
00724995317652V. MuellerOP193OP1932026-10-15

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00190776434168MillenniumAvalign Technologies, Inc.KAD2026-10-09
G2231337690Medetz Surgical InstrumentsMedetz Surgical Instruments LLCKAD2026-10-01
00724995270704V. MuellerSTERIS Deutschland GmbHKAD2026-09-25
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04054462905584evonosevonos GmbH & Co. KGKAD2026-08-21
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