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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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  • MD Atlas
  • ACIME FRAME

Data from EUDAMED, last updated May 19, 2026

DUAD-STD-AC

376036546DUAD-STD-ACGJ

2 references

Class I
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Risk category
Class I
Manufacturer
ACIME FRAME

Device family identification

Device name
—
Basic UDI-DI
376036546DUAD-STD-ACGJ
Device model
DUAD-STD-AC
Issuing agency
GS1
Version date
May 9, 2022

Classification

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

Manufacturer

Manufacturer

Name
ACIME FRAME
SRN
FR-MF-000016067
Country
France
Email
contact@acimeframe.com

Device characteristics

Active device

EMDN code(s)

European Medical Device Nomenclature — the EU product classifications carried across this device family's references.

  • V080603Treatment, diagnosis and monitoring medical beds

References by status

References

2 references

Export results

Applied filters

  • basicUdiUlid·01G2MBG369GESGJ3WR20E6EF91

Format

Summary

31 columns included
  • Trade name
  • Basic UDI-DI
  • UDI-DI code
  • Risk category
  • Applicable legislation
  • Status
  • Organization name
  • SRN
  • Reference / catalog number
  • Additional product description
  • Intended medical purpose
  • Market country
  • Issuing entity
  • Market info update date
  • Sterile
  • Single use
  • Contains latex
  • Reprocessed single-use
  • Direct marking
  • CMR substance
  • Endocrine disruptor
  • Annex XVI applicable
  • Sterilization
  • OEM applicable
  • EMDN codes
  • Last updated
  • Basic UDI-DI device name
  • Basic UDI-DI device model
  • Basic UDI-DI implantable
  • Basic UDI-DI reagent
  • DM Atlas link
Trade nameReference / catalog numberUDI-DI codeQuantityStatus
DUA ELECTRADUAD010037603654601051On the market
DUA FEMINADUAD007037603654600751On the market