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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
  • Xiamen Neaq Imp.& Exp. Co., Ltd

Data from EUDAMED, last updated Jun 11, 2026

NQF001,NQF002,NQF003,NQF004,NQF005,NQF006,NQF007,NQF008,NQF009,NQF010,NQF011,NQF012,NQF013,NQF014,NQF015,NQF016,NQF017,NQF018,NQF019,NQF020,NQF021,NQF022,NQF023,NQF024,NQF025,NQF026,NQF027,NQF028,NQF029,NQF030, NQS007-2 ,NQE031-4,SC6063AL,NQGB001,NQD001

697680164GRABBARX4

33 references

Class I
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Risk category
Class I
Manufacturer
Xiamen Neaq Imp.& Exp. Co., Ltd

Device family identification

Device name
—
Basic UDI-DI
697680164GRABBARX4
Device model
NQF001,NQF002,NQF003,NQF004,NQF005,NQF006,NQF007,NQF008,NQF009,NQF010,NQF011,NQF012,NQF013,NQF014,NQF015,NQF016,NQF017,NQF018,NQF019,NQF020,NQF021,NQF022,NQF023,NQF024,NQF025,NQF026,NQF027,NQF028,NQF029,NQF030, NQS007-2 ,NQE031-4,SC6063AL,NQGB001,NQD001
Issuing agency
GS1
Version date
May 7, 2026

Classification

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

Manufacturer & authorised representative

Manufacturer

Name
Xiamen Neaq Imp.& Exp. Co., Ltd
SRN
CN-MF-000037906
Country
China
Email
helen.fan@xmneaq.com

Authorised representative

Name
SUNGO Europe B.V.
SRN
NL-AR-000000247
Country
Netherlands

Device characteristics

No device characteristics flagged

EMDN code(s)

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

  • Y181809Armrests

References by status

References

33 references

Export results

Applied filters

  • basicUdiUlid·01KR0JJK9D4Q1K07M3ZKTP366H

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
NQF006NQF006069768016450511On the market
NQF008NQF008069768016450751On the market
NQF015NQF015069768016451431On the market
NQGB001NQGB001069768016453341On the market
NQF004NQF004069768016450371On the market
NQF024NQF024069768016452351On the market
NQF019NQF019069768016451811On the market
NQF002NQF002069768016450131On the market
SC6063ALSC6063AL069768016453271On the market
NQF023NQF023069768016452281On the market
NQF017NQF017069768016451671On the market
NQF005NQF005069768016450441On the market
NQF025NQF025069768016452421On the market
NQF022NQF022069768016452111On the market
NQF020NQF020069768016451981On the market
NQF021NQF021069768016452041On the market
NQF027NQF027069768016452661On the market
NQF003NQF003069768016450201On the market
NQF028NQF028069768016452731On the market
NQF009NQF009069768016463171On the market
NQF029NQF029069768016452801On the market
NQF007NQF007069768016450681On the market
NQF018NQF018069768016451741On the market
NQD001NQD001069768016453411On the market
NQF026NQF026069768016452591On the market