Pricing Sign in

Role
Country
Date of registration
Address

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.

Organization name
UDI-DI code
Reference / catalog number

AnGer Serrated Interproximal… — Class I MDR

MD Atlas
AnGer G&A Przedsiębiorstwo Produkcyjne

EUDAMED last updated this device on Dec 18, 2025

AnGer Serrated Interproximal Strip 120mm x 6mm x 0,05mm

590761904010EL

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: AnGer G&A Przedsiębiorstwo Produkcyjne
UDI-DI code: 05907619046267
Reference / catalog number: 1219

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?

View device family (Basic UDI)

Manufacturer information

Organization name: AnGer G&A Przedsiębiorstwo Produkcyjne
SRN: PL-MF-000001898
Manufacturer status: Active

Related devices

Art.33-74 Polyester Crown Forms, Lower Canine, size 74, Left, 5pcs590761904001EKOn the market Art.33-90 Polyester Crown Forms, Lower Canine, size 90, Left, 5pcs590761904001EKOn the market Art.41-54 Polyester Crown Forms, Lower Incisor Central, size 54, Right, 5pcs590761904001EKOn the market Elastic Interdental Wedges - Colour-coded, Assortment - six sizes, 240pcs590761904014EUOn the market Flat Polyester Matrices, shape #1, 0.050mm, 50pcs590761904002EMOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Critical warnings

4 warnings recorded — scroll inside the panel to see all entries.

CW029
EUDAMED did not publish a description for this code.
CW318
EUDAMED did not publish a description for this code.
CW218
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.

EasyUDICompliance engine

Sponsored

Your devices, UDI-compliant — without drowning in regulation

EUDAMED-ready· UDI-enriched

Basic UDIUDI-DIUDI-PIAttributeDocument

Print-ready label

From your product file — no manual entry

Exclusive to MD Atlas usersClaim my −20% discount

by Made In Tracker

Market distribution

Primary placement in Poland; available across 1 country total.

Placed on the market in Poland; per-country availability dates not published.

Device identification

Trade name: AnGer Serrated Interproximal Strip 120mm x 6mm x 0,05mm
UDI-DI code: 05907619046267
Basic UDI-DI: 590761904010EL
Reference / catalog number: 1219
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 10
Additional product description: AnGer Serrated Interproximal Strip 120mm x 6mm x 0,05mm; 10pcs
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05907619046267

Sign in to download the DataMatrix

Create a free account to download the UDI-DI DataMatrix for this device.

Email

Password

No account yet?

UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

Sign in to generate the UDI-PI DataMatrix

Create a free account, then generate the compliant UDI-PI carrier for this device.

Email

Password

No account yet?

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Q019003DENTAL FLOSS AND OTHER DEVICES FOR ORAL HYGIENE (FOR PROFESSIONAL USE)

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

Become a partner of MD Atlas