Flux-C Cervical Interbody

Primary DI
00810076330051
Brand
Flux-C Cervical Interbody
Company
Ulrich Medical Usa, Inc.
Model
UU081-00-1211-10
Catalog number
UU081-00-1211-10
Device description
3D Porous Titanium Cervical Interbody, 12x11mm, 10mm height, 0°
Published
2022-09-08
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
ODPIntervertebral Fusion Device With Bone Graft, Cervical

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
ODPIntervertebral Fusion Device With Bone Graft, CervicalOrthopedic2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00810076330051PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00810076330051008100763300518100763300510810076330051

GMDN Terms#

Term, Definition table
TermDefinition
Metallic spinal interbody fusion cageA device intended to be implanted into the space of an intervertebral disc that has been partially or totally removed during surgery in order to allow bone fusion between two contiguous vertebral bodies, typically in the treatment of degenerative disc disease (DDD). It is in the form of a hollow, porous, threaded and/or fenestrated cylindrical or geometrical device made of metal [e.g., titanium (Ti)] that provides mechanical stability and sufficient space for therapeutic spinal bone fusion to occur; bone graft is typically used to help with osseointegration. Fixation screws and devices associated with implantation may be included with the device.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
636-519-0268info@ulrichmedicalusa.com

Regulatory Flags#

DUNS number
624083866
Device count
1
DM exempt
false
Premarket exempt
false
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
00810076338347Momentum UU051-10-45252026-03-20
00810076338354Momentum UU051-10-45302026-03-20
00810076339467Momentum UU051-10-45352026-03-20
00810076339474Momentum UU051-10-45402026-03-20
00810076339481Momentum UU051-10-45452026-03-20
00810076339498Momentum UU051-10-45502026-03-20
00810076339504Momentum UU051-11-45252026-03-20
00810076339511Momentum UU051-11-45302026-03-20
00810076339528Momentum UU051-11-45352026-03-20
00810076339535Momentum UU051-11-45402026-03-20
00810076339542Momentum UU051-11-45452026-03-20
00810076339559Momentum UU051-11-45502026-03-20
00810076338545Momentum MIS - Modified InstrumentUU994-96-012026-03-02
00814386029902Momentum UU052-50-00322026-03-02
00810076338248Momentum UU052-85-00202025-07-19
00810076338255Momentum UU052-85-00302025-07-19
00810076338262Momentum UU052-85-00402025-07-19
00814386024679Momentum UU051-72-35602025-07-19
00814386024709Momentum UU051-74-35552025-07-19
00814386024716Momentum UU051-74-35602025-07-19

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