PERCUTANEOUS REAMER

Primary DI
03700879513874
Brand
PERCUTANEOUS REAMER
Company
NOVASTEP
Model
CRE13030
Catalog number
CRE13030
Device description
Sterile Shannon X-Larga Ø3.0 x 30 mm
Published
2021-04-08
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
HWEInstrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HWEInstrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/AttachmentGeneral, Plastic Surgery1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
03700879513874PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
03700879513874037008795138743700879513874

GMDN Terms#

Term, Definition table
TermDefinition
Orthopaedic bur, single-useA sterile, rotary cutting device consisting of a shaft of high-grade steel and a cutting head of hard metal/material with fluting or cutting planes of various shapes at the working end and which is designed to fit into an appropriate powered handpiece that provides the rotation allowing the user to excavate/shape bone tissue during small and large bone surgery (e.g., maxillofacial, spinal, or orthopaedic). This is a single-use device.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+33299338650contact@novastep-ortho.com
+33299338650regulatory-IntFA@enovis.com

Regulatory Flags#

DUNS number
264255288
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
true
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
03700879518565PECAPLASTY®ACC1025P0001ACC1025P00012026-03-19
03700879518572PECAPLASTY®ACC1025P0002ACC1025P00022026-03-19
03700879518589PECAPLASTY®XMS01055-1XMS01055-12026-03-19
03700879518596PECAPLASTY®XMS01055-2XMS01055-22026-03-19
03700879515151PECA®2.0PS060118PS0601182025-11-07
03700879515168PECA®2.0PS060120PS0601202025-11-07
03700879515175PECA®2.0PS060122PS0601222025-11-07
03700879515182PECA®2.0PS060124PS0601242025-11-07
03700879515199PECA®2.0PS060126PS0601262025-11-07
03700879515205PECA®2.0PS060128PS0601282025-11-07
03700879515212PECA®2.0PS060130PS0601302025-11-07
03700879515229PECA®2.0PS060132PS0601322025-11-07
03700879515236PECA®2.0PS060134PS0601342025-11-07
03700879515243PECA®2.0PS060136PS0601362025-11-07
03700879515250PECA®2.0PS060138PS0601382025-11-07
03700879515267PECA®2.0PS060140PS0601402025-11-07
03700879515274PECA®2.0PS060142PS0601422025-11-07
03700879515281PECA®2.0PS060144PS0601442025-11-07
03700879515298PECA®2.0PS060146PS0601462025-11-07
03700879515304PECA®2.0PS060148PS0601482025-11-07

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