Organization name

MANI, INC.

SRN

JP-MF-000017860

Manufacturer status

Active

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

• Do not resterilize
• Do not use if package is damaged
• Do not re-use

Primary placement in Germany; available across 32 countries total.

Trade name

MANI SUTURES NYLON - 10-0 NYLON

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.

04546951634100

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.

4546951000006ZK

Reference / catalog number

2002S

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 IIb

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

MANI Ophthalmic Sutures

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

• 6.5mm
• Suture Length 15cm

1 packaging level registered — each level carries its own UDI-DI.

• 04546951634100× 1 unitBase unit
  • 14546951634107× 12 units

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

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

• H010201010101POLYAMIDE MONOFILAMENT WITH NEEDLE

• Class IIb medical devices in EUDAMED

Certificate health across this manufacturer's portfolio.

No certificate specifically references this device's Basic UDI-DI.