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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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b.Bone — 83 UDI-DI variants, MDR (GreenBone Ortho Spa)

MD Atlas
GreenBone Ortho Spa

Data from EUDAMED, last updated May 30, 2026

b.Bone

805384834IP01R3D01M01DD

83 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class III

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Manufacturer: GreenBone Ortho Spa

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Device characteristics

Implantable

Legacy certificates

Certificate number: 044-00-01-MDR
Type: refdata.certificate-mdr-type.technical-documentation
Notified body: ITALCERT SRL (0426)
Validity: Apr 20, 2026 → Mar 5, 2029

Identity & classification

Basic UDI-DI: 805384834IP01R3D01M01DD
Device name: b.Bone
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Version date: Mar 13, 2024

Manufacturer & authorised representative

Manufacturer

Name: GreenBone Ortho Spa
SRN: IT-MF-000033034
Country: Italy
Email: info@greenbone.it
Phone: +39 054646666

Variants by status

UDI-DI variants

83 UDI-DI variants

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Applied filters

basicUdiUlid01HRW7MY8568YWVNGERKNWKW8B

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

GR051010PS08053848340472
HC100040PS 08053848341288
HP401010PS08053848341646
b.Bone08053848341486
HC150660PS 08053848340564
HP200510PS08053848341431
HP201530PS 08053848341516
HP401530PS08053848341691

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