FDA.reportPublic FDA data

V. Mueller

Primary DI
10885403010149
Brand
V. Mueller
Company
CAREFUSION 2200, INC
Model
AU12810
Catalog number
AU12810
Device description
V. Mueller SCHEER MICRO WIRE CRIMPING FORCEPS SMOOTH JAWS, LENGTH 5MM OVERALL LENGTH 5" (12.7CM)
Published
2018-07-13
Public version status
Update
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
NNNCRIMPER, WIRE, ENT, NON-STERILE

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
NNNCrimper, Wire, Ent, Non-SterileEar, Nose, Throat1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10885403010149PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized table
Source identifierGTIN-14 normalized
1088540301014910885403010149

GMDN Terms#

Term, Definition table
TermDefinition
Surgical soft-tissue manipulation forceps, alligator, reusableA long, thin, hand-held manual surgical instrument designed to facilitate grasping and manipulation of soft-tissues/anatomical structures [typically during ear/nose/throat (ENT) surgery]; it is not intended for insertion through an endoscope, nor into the eye. Commonly referred to as alligator- or crocodile-forceps, it has a slender body (to allow for restricted access) and small grasping blades which are hinged close to the distal (working) end. It is a metallic device available in various sizes/lengths; some types may include an integrated suction channel. This is a reusable device intended to be sterilized prior to use.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1(800)323-9088Customer_Support@BD.com
+1(800)548-4873xx@xx.xx

Regulatory Flags#

DUNS number
832696038
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
50382909101206Surgiphor9101209101202026-03-05
10885403273780PleurX50-007550-00752017-06-12
10885403075964PleurX50-905050-90502017-06-12
50885403075993Denver42-200042-20002017-06-12
50885403076006Denver42-205542-20552017-06-12
50885403076082Denver42-205042-20502017-06-12
10885403051722V. MuellerHY21305HY213052017-08-11
10885403049408V. MuellerGU4050-008GU4050-0082018-08-30
10885403071263V. MuellerNL1350NL13502018-09-05
10885403105159V. MuellerOS5000-002OS5000-0022018-09-10
20885403473170N/A5513E5513E2019-03-25
50885403142176Wet Exidine448944892018-07-18
50885403142183NA442044202018-07-18
50885403142190NA4461A4461A2018-07-18
50885403142220NA4472A4472A2018-07-18
50885403175211NA443744372018-07-18
50885403184473NA446844682018-07-18
50885403184480NA4469A4469A2018-07-18
50885403192829Scrub Care ExidineCLEAN1CLEAN12018-05-02
10885403465154Snowden-PencerSI325SI3252018-01-16

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Primary DI, Brand, Company table
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G586E7212450Novo SurgicalNOVO SURGICAL, INC.NNN2023-12-18
00190776318871MillenniumAvalign Technologies, Inc.NNN2023-11-13
00190776043605AvalignAvalign Technologies, Inc.NNN2023-09-28
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00190776318840MILLENNIUMAvalign Technologies, Inc.NNN2023-09-28
54026704804233PILLINGTELEFLEX INCORPORATEDNNN2022-12-08
54026704804226PILLINGTELEFLEX INCORPORATEDNNN2022-12-08
54026704804271PILLINGTELEFLEX INCORPORATEDNNN2022-12-08
00842331174704Novo Surgical Inc. NOVO SURGICAL, INC.NNN2022-11-14
00842331177682Novo Surgical Inc. NOVO SURGICAL, INC.NNN2022-11-14
00842331186219Novo Surgical Inc. NOVO SURGICAL, INC.NNN2022-11-14
00842331146206Novo Surgical Inc. NOVO SURGICAL, INC.NNN2022-11-11
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00190660072797Ambler SurgicalAMBLER SURGICAL CORP.NNN2021-01-07
04046964589188AESCULAPAESCULAP, INC.NNN2020-05-08
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