FX Solutions® 903-0046

GUDID 03701037314340

HUMELOCK REVERSED GLENOID MANUAL REAMER Ø32mm

FX SOLUTIONS

Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable
Primary Device ID03701037314340
NIH Device Record Keye2572fdb-30ed-4fe0-be40-82e059d73be1
Commercial Distribution StatusIn Commercial Distribution
Brand NameFX Solutions®
Version Model Number903-0046
Catalog Number903-0046
Company DUNS263076196
Company NameFX SOLUTIONS
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Store away from light and sunlight Store away from moisture
Special Storage Condition, SpecifyBetween 0 and 0 *Store away from light and sunlight Store away from moisture
Special Storage Condition, SpecifyBetween 0 and 0 *Store away from light and sunlight Store away from moisture
Special Storage Condition, SpecifyBetween 0 and 0 *Store away from light and sunlight Store away from moisture
Special Storage Condition, SpecifyBetween 0 and 0 *Store away from light and sunlight Store away from moisture
Special Storage Condition, SpecifyBetween 0 and 0 *Store away from light and sunlight Store away from moisture
Special Storage Condition, SpecifyBetween 0 and 0 *Store away from light and sunlight Store away from moisture
Special Storage Condition, SpecifyBetween 0 and 0 *Store away from light and sunlight Store away from moisture
Special Storage Condition, SpecifyBetween 0 and 0 *Store away from light and sunlight Store away from moisture
Special Storage Condition, SpecifyBetween 0 and 0 *Store away from light and sunlight Store away from moisture
Special Storage Condition, SpecifyBetween 0 and 0 *Store away from light and sunlight Store away from moisture
Special Storage Condition, SpecifyBetween 0 and 0 *Store away from light and sunlight Store away from moisture
Special Storage Condition, SpecifyBetween 0 and 0 *Store away from light and sunlight Store away from moisture
Special Storage Condition, SpecifyBetween 0 and 0 *Store away from light and sunlight Store away from moisture
Special Storage Condition, SpecifyBetween 0 and 0 *Store away from light and sunlight Store away from moisture

Device Identifiers

Device Issuing AgencyDevice ID
GS103701037314340 [Primary]
GS103701037314340 [Primary]
GS103701037314340 [Primary]
GS103701037314340 [Primary]
GS103701037314340 [Primary]
GS103701037314340 [Primary]
GS103701037314340 [Primary]
GS103701037314340 [Primary]
GS103701037314340 [Primary]
GS103701037314340 [Primary]
GS103701037314340 [Primary]
GS103701037314340 [Primary]
GS103701037314340 [Primary]
GS103701037314340 [Primary]
GS103701037314340 [Primary]

FDA Product Code

LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[03701037314340]

Moist Heat or Steam Sterilization


[03701037314340]

Moist Heat or Steam Sterilization


[03701037314340]

Moist Heat or Steam Sterilization


[03701037314340]

Moist Heat or Steam Sterilization


[03701037314340]

Moist Heat or Steam Sterilization


[03701037314340]

Moist Heat or Steam Sterilization


[03701037314340]

Moist Heat or Steam Sterilization


[03701037314340]

Moist Heat or Steam Sterilization


[03701037314340]

Moist Heat or Steam Sterilization


[03701037314340]

Moist Heat or Steam Sterilization


[03701037314340]

Moist Heat or Steam Sterilization


[03701037314340]

Moist Heat or Steam Sterilization


[03701037314340]

Moist Heat or Steam Sterilization


[03701037314340]

Moist Heat or Steam Sterilization


[03701037314340]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-10-16
Device Publish Date2020-10-08

On-Brand Devices [FX Solutions®]

03701037312674HUDSON EXTENSION CONNECT
03701037312667RATCHET T-HANDLE / HUDSON
03701037312650HANDLE / HUDSON
03701037312643RATCHET HANDLE / HUDSON
03701037312636DRILLING GUIDE DEPTH GAUGE
03701037312629LONG IMPACTEUR DE METAGLENE
0370103731261240/16 HUMELOCK REVERSED BROACH
0370103731260540/14 HUMELOCK REVERSED BROACH
0370103731259940/12 HUMELOCK REVERSED BROACH
0370103731258236/14 HUMELOCK REVERSED BROACH
0370103731257536/12 HUMELOCK REVERSED BROACH
0370103731256836/10 HUMELOCK REVERSED BROACH
0370103731255132/12 HUMELOCK REVERSED BROACH
0370103731254432/10 HUMELOCK REVERSED BROACH
0370103731253732/08 HUMELOCK REVERSED BROACH
03701037312520HUMELOCK REVERSED SUPERIOR LATERAL CUTTING GUIDE
03701037312513HUMELOCK REVERSED LEFT DELTO PECTORAL CUTTING GUIDE
03701037312506HUMELOCK REVERSED RIGHT DELTO PECTORAL CUTTING GUIDE
03701037312490145° EXTRAMEDULLARIS DELTO PECTORAL CUTTING GUIDE
03701037312483LARGE AIMER
03701037312438SYMETRIC GLENOID WITH SPIKES K-WIRE GUIDE + TEMPLATE SIZE L
03701037312421SYMETRIC GLENOID WITH SPIKES K-WIRE GUIDE + TEMPLATE SIZE M
03701037312414SYMETRIC GLENOID WITH SPIKES K-WIRE GUIDE + TEMPLATE SIZE S
03701037312407SYMETRIC GLENOID WITH SPIKES K-WIRE GUIDE + TEMPLATE SIZE XS
03701037312391POSTERIOR GLENOID RETRACTOR
03701037312384HUMELOCK REVERSED LEFT DELTO PECTORAL CUTTING GUIDE
03701037312377135° EXTRAMEDULLARIS DELTO PECTORAL CUTTING GUIDE
03701037312360HUMELOCK REVERSED RIGHT DELTO PECTORAL CUTTING GUIDE
03701037312353RASP HANDLE
03701037312346LONG STOP DRILL BIT Ø7.5mm
03701037312339HANDLE BIT / FX / HUDSON
03701037312322LONG GUIDE Ø10mm
03701037312315CANNULATED 3,5MM HEX. SCREWDRIVER BIT / HUDSON
03701037312308STEM IMPACTOR
03701037312292GLENOID RESURFACING REAMER Ø39 mm / FX
03701037312285GLENOID RESURFACING REAMER Ø35 mm / FX
03701037312278GLENOID RESURFACING REAMER Ø31 mm / FX
03701037312261GLENOID RESURFACING REAMER Ø27 mm / FX
03701037312254DRILL BIT Ø3,2mm L271mm/AO
03701037312247STOP DRILL BIT Ø7.5 mm L.150 mm / HUDSON
03701037312230STOP DRILL BIT Ø5.0 mm L.150 mm / HUDSON
03701037312223STOP DRILL BIT Ø5.0 mm L.40 mm / FX
03701037312216HANDLE BIT RELEASE/ FX / HUDSON
03701037312209GLENOID RESURFACING REAMER Ø43 mm / FX
03701037312193OFFSET SCREWED PROTECTOR Ø46mm 
03701037312186OFFSET SCREWED PROTECTOR Ø41mm 
03701037312155LONG GUIDES HOLDER
03701037312148K-WIRE GUIDE WITH GAUGE
03701037312131K-WIRE GUIDE WITHOUT GAUGE
03701037312124GLENOID RESURFACING REAMER Ø36mm WITH DRILL /HUDSON

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