Organization name

TI Medical Private Limited

SRN

IN-MF-000026561

Manufacturer status

Active

1 warning recorded — scroll inside the panel to see all entries.

• Do not use if package is damaged

Primary placement in Germany; available across 32 countries total.

Trade name

Mass

UDI-DI code

Primary DI

The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.

08904248207059

Basic UDI-DI

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

89042482MAS005HX

Reference / catalog number

TI/C-BRO/01

Issuing entity

UDI issuing entities

Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.

GS1

Risk category

MDR risk classes

MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.

Class III

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

Absorbable Surgical Suture

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

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

• H010101010101POLYDIOXANONE MONOFILAMENT WITH NEEDLE FOR OPEN SURGERY

• Class III medical devices in EUDAMED

Certificate health across this manufacturer's portfolio.