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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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  • GIMA SPA

Data from EUDAMED, last updated May 31, 2026

ISTEROMETRO RIUTILIZZABILE

802327900L0311022900000Q2

2 references

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

Device family identification

Device name
ISTEROMETRO RIUTILIZZABILE
Basic UDI-DI
802327900L0311022900000Q2
Device model
ISTEROMETRO RIUTILIZZABILE
Issuing agency
GS1
Version date
May 28, 2026

Classification

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

Manufacturer

Manufacturer

Name
GIMA SPA
SRN
IT-MF-000011004
Country
Italy
Email
REGOLATORIO@GIMAITALY.COM
Phone
029538541

Device characteristics

No device characteristics flagged

EMDN code(s)

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

  • L031102Exploration probes, reusable

References by status

References

2 references

Export results

Applied filters

  • basicUdiUlid·01KSQAP20S4DGERJPRPRFCJ113

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
2681626816080232792681641On the market
2680426804080232792680411On the market