Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ 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

Hygiene Sleeve for Bite Cover — Class I MDR by M. G. Kurth GmbH

MD Atlas
M. G. Kurth GmbH

EUDAMED last updated this device on May 21, 2026

Hygiene Sleeve for Bite Cover

++G086HygieneSleevesLC

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: M. G. Kurth GmbH
UDI-DI code: ++086703031
Reference / catalog number: 70303

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?

Manufacturer information

Organization name: M. G. Kurth GmbH
SRN: DE-MF-000045501
Manufacturer status: Active

Related devices

80974++G086AnmischblocksDJOn the market 80975++G086AnmischblocksDJOn the market 80845++G086AnmischblocksDJOn the market 80840++G086AnmischblocksDJOn the market 80873++G086AnmischblocksDJOn the market

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: Hygiene Sleeve for Bite Cover
UDI-DI code: ++086703031
Basic UDI-DI: ++G086HygieneSleevesLC
Reference / catalog number: 70303
Issuing entity: HIBCC

Classification

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

Device details

Quantity: 200
Additional product description: —
Additional information URL: https://www.mgk-kurth.com/ifu/
Clinical sizes: 4 MU10
8 MU10

EMDN nomenclature code(s)

T030102COVER SHEATHS, INSTRUMENTS AND EQUIPMENTS

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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.