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

DHC PACKOT — Class I MDR by ACIME FRAME

MD Atlas
ACIME FRAME

EUDAMED last updated this device on May 6, 2022

DHC PACKOT

376036546PACK-STD-ACFM

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ACIME FRAME
UDI-DI code: 03760365460518
Reference / catalog number: PACK051

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: ACIME FRAME
SRN: FR-MF-000016067
Manufacturer status: Active

Related devices

AKU VUE376036546FUSI-STD-AC2GOn the market ALCYONE 3376036546SKIF-STD-NIWJOn the market AMBU FUSION +376036546FUSI-STD-AC2GOn the market AMBU FUSION 2376036546FUSI-STD-AC2GOn the market AMBU FUSION A376036546FUSI-STD-AC2GOn 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.

Market distribution

Primary placement in France; available across 1 country total.

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

Device identification

Trade name: DHC PACKOT
UDI-DI code: 03760365460518
Basic UDI-DI: 376036546PACK-STD-ACFM
Reference / catalog number: PACK051
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: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V08020101GENERIC USE ELECTRIC MEDICAL CHAIRS

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