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Single-use 10mm delivery and sampling kit

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref NOXKIT-1-10

by NOxBOX Limited

Identity

Trade Name
Single-use 10mm delivery and sampling kit EUDAMED
NOxBOXi FDA UDI
Generic Name
Nitric oxide delivery unit, system-based FDA UDI
Device Name
NOxBOXi Consumable Kits EUDAMED
Single-use 10mm delivery and sampling kit EUDAMED
Single use 10mm delivery and sampling kit FDA UDI
Model / Reference
NOXKIT-1-10 EUDAMEDFDA UDI
Description
Single use 10mm delivery and sampling kit FDA UDI

Identifiers

Catalog Number
NXBNOXKIT-1-10 FDA UDI
Primary DI / UDI-DI
05060541640054 EUDAMEDFDA UDI
Basic UDI-DI
506054164NBiKITSMR EUDAMED
B-05060541640054 EUDAMED
510(k) Number
K171696 FDA UDI
FDA Product Code
CCL FDA UDI
MRQ FDA UDI
MRP FDA UDI
MRO FDA UDI
MRN FDA UDI
EMDN Code
Z1203019002,Z1203019085 EUDAMED
GMDN Term
Nitric oxide delivery unit, system-based FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
868.1720 FDA UDI
868.2385 FDA UDI
868.2380 FDA UDI
868.5165 FDA UDI
Market of Registration
Northern Ireland EUDAMED
Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Single-use 10mm delivery and sampling kit by NOxBOX Limited — Class IIa — MDD, MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
NOxBOX Limited
EUDAMED SRN
GB-MF-000009734
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (3)

  • EUDAMED e6bb38c0-7ad4-434e-a086-b5646d866d73 61 fields · synced Jul 17, 2026
  • EUDAMED 40f331fe-9497-4fce-be1a-f53beca189bb 61 fields · synced May 19, 2026
  • FDA UDI b0e07c51-720d-4a07-8bae-481659da9b5b 37 fields · synced May 30, 2026