Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

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

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Reamer, Acorn, Thin Shaft, Fully… — 45 UDI-DI variants, MDR

MD Atlas
Medos International SARL

Data from EUDAMED, last updated May 23, 2026

Reamer, Acorn, Thin Shaft, Fully Fluted, Low Profile

0886705a00064KH

45 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Medos International SARL

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

ReusableMeasuring function

Identity & classification

Basic UDI-DI: 0886705a00064KH
Device name: Reamer, Acorn, Thin Shaft, Fully Fluted, Low Profile
Device model: Reamers
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Dec 30, 2025

Manufacturer & authorised representative

Manufacturer

Name: Medos International SARL
SRN: CH-MF-000014268
Country: Switzerland
Email: EUDAMED_Enquiries@its.jnj.com
Phone: +41 32 934 80 00

Authorised representative

Name: DePuy Ireland UC
SRN: IE-AR-000009328
Country: Ireland
Phone: +353 (0)21 4914000

Variants by status

UDI-DI variants

45 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KDR057WQBX21V8TNYSSQC1JM

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

ACORN REAMER, STERILE10886705011216
ACORN REAMER, STERILE10886705011186
ACORN REAMER, STERILE10886705011223
ACORN REAMER, STERILE10886705011131
ACORN REAMER, STERILE10886705011155
ACORN REAMER, STERILE10886705011230
ACORN REAMER, STERILE10886705011162
ACORN REAMER, STERILE10886705011124
ACORN REAMER, STERILE10886705011148
ACORN REAMER, STERILE10886705011209
ACORN REAMER, STERILE10886705011193
ACORN REAMER, STERILE10886705011179
ACORN REAMER, STERILE10886705011247
RESTORE ACORN REAMER/THIN SHAFT10886705005796
RESTORE ACORN REAMER/THIN SHAFT10886705005789
RESTORE ACORN REAMER/THIN SHAFT10886705006687
RESTORE ACORN REAMER/THIN SHAFT10886705006694
RESTORE ACORN REAMER/THIN SHAFT10886705005819
RESTORE ACORN REAMER/THIN SHAFT10886705005833
RESTORE ACORN REAMER/THIN SHAFT10886705005826
RESTORE ACORN REAMER/THIN SHAFT10886705005772
RESTORE ACORN REAMER/THIN SHAFT10886705005802
RESTORE ACORN REAMER/THIN SHAFT10886705006724
RESTORE ACORN REAMER/THIN SHAFT10886705006731
RESTORE ACORN REAMER/THIN SHAFT10886705005840

1 2