FDA.reportPublic FDA data

BRM BIOPLAN INSTRUMENT

Primary DI
08057717553680
Brand
BRM BIOPLAN INSTRUMENT
Company
BRM EXTREMITIES SRL
Model
Bioplan - Trial Size 10
Catalog number
SBPI10P010
Published
2026-08-18
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
LXHOrthopedic Manual Surgical Instrument

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LXHOrthopedic Manual Surgical InstrumentOrthopedic1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
08057717553680PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
08057717553680080577175536808057717553680

GMDN Terms#

Term, Definition table
TermDefinition
Orthopaedic prosthesis implantation positioning instrument, reusableA hand-held surgical instrument intended to be used during implantation of an orthopaedic prosthesis, either manually or as a computer-assisted surgery (CAS) device, to aid in the navigation/placement of the prosthesis or other instruments [e.g., drill sleeves and guide wires (Kirschner wires), patella saw guide]. It may be used for the following applications: 1) to hold/align/fix/guide other instruments, prostheses, or prosthesis components; 2) to provide relative position landmarks; 3) to ascertain correct spatial orientation or limb alignment; and/or 4) as an interface (non-adaptive) between prosthesis components. This is a reusable device intended to be sterilized prior to use.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Special Storage Condition, Specify00Keep at room temperature and away from direct sources of light

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+3903411693087info@brm-extremities.com

Regulatory Flags#

DUNS number
435126746
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
true
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
08053782781652Bioplan Instruments KitInstruments kit for the implant of BRM ExtremitiesKIT.BIOPLAN2026-08-18
08057717553635BRM BIOPLAN INSTRUMENTScrewdriver – BioplanSBPI1CI0012026-08-18
08057717553642BRM BIOPLAN INSTRUMENTExtractor Screwdriver - BioplanSBPI1CE0022026-08-18
08057717553659BRM BIOPLAN INSTRUMENTBioplan - Trial Size 7SBPI10P0072026-08-18
08057717553666BRM BIOPLAN INSTRUMENTBioplan - Trial Size 8SBPI10P0082026-08-18
08057717553673BRM BIOPLAN INSTRUMENTBioplan - Trial Size 9SBPI10P0092026-08-18
08057717553697BRM BIOPLAN INSTRUMENTBioplan - Trial Size 11SBPI10P0112026-08-18
08057717553703BRM BIOPLAN INSTRUMENTBioplan - Trial Size 12SBPI10P0122026-08-18
08057717553710BRM BIOPLAN INSTRUMENTBioplan - Trial Size 13SBPI10P0132026-08-18
08057717553727BRM BIOPLAN INSTRUMENTProbe – BioplanSBPI10S0012026-08-18
08057717553734BRM BIOPLAN INSTRUMENTGuide wire Ø 2 mm - BioplanSBPI1PG0012026-08-18
08057717553741BRM BIOPLAN INSTRUMENTPush wireSBPI1SF0012026-08-18
08057717553758BRM BIOPLAN INSTRUMENTSBioplan Sterilization TraySBPI000000B2026-08-18
08053782783755Bioplan Titanium implantBioplan Titanium implant 7DBI1070132026-08-14
08053782783762Bioplan Titanium implantBioplan Titanium implant 8DBI1080142026-08-14
08053782783779Bioplan Titanium implantBioplan Titanium implant 9DBI1090152026-08-14
08053782783786Bioplan Titanium implantBioplan Titanium implant 10DBI1100162026-08-14
08053782783793Bioplan Titanium implantBioplan Titanium implant 11DBI1110172026-08-14
08053782783809Bioplan Titanium implantBioplan Titanium implant 12DBI1120182026-08-14
08053782783816Bioplan Titanium implantBioplan Titanium implant 13DBI1130192026-08-14

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Primary DI, Brand, Company table
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00888867552692Arthrex®ARTHREX, INC.LXH2026-09-18
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00888867552722Arthrex®ARTHREX, INC.LXH2026-09-18
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00888867552760Arthrex®ARTHREX, INC.LXH2026-09-18
00888867574564Arthrex®ARTHREX, INC.LXH2026-09-18
00888867574571Arthrex®ARTHREX, INC.LXH2026-09-18
00888867574588Arthrex®ARTHREX, INC.LXH2026-09-18
04054896000831Control GaugesSilony Medical GmbHLXH2026-09-18
04054896000855Implant ModifierSilony Medical GmbHLXH2026-09-18
04054896000862Implant ModifierSilony Medical GmbHLXH2026-09-18
04054896000879Implant ModifierSilony Medical GmbHLXH2026-09-18
04054896000886Forceps and ClampsSilony Medical GmbHLXH2026-09-18
04054896000893(Re-) Positioning ToolsSilony Medical GmbHLXH2026-09-18
04054896000909(Re-) Positioning ToolsSilony Medical GmbHLXH2026-09-18
04054896000916(Re-) Positioning ToolsSilony Medical GmbHLXH2026-09-18
04054896000923AdapterSilony Medical GmbHLXH2026-09-18