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D-lite++ Patient Spirometry Set, 2 m/7 ft

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 2104297-001

by GE Healthcare Finland Oy

Identity

Trade Name
NA FDA UDI
Generic Name
Gas-sampling/monitoring respiratory tubing, single-use FDA UDI
Device Name
D-lite++ Patient Spirometry Set, 2 m/7 ft EUDAMED
D-LITE++ PATIENT SPIROMETRY SET, 2M/7FT, 1 PCS FDA UDI
Model / Reference
2104297-001 EUDAMED
D-LITE PATIENT SPIROMETRY SET 2104297-001 FDA UDI
Description
D-LITE++ PATIENT SPIROMETRY SET, 2M/7FT, 1 PCS FDA UDI

Identifiers

Primary DI / UDI-DI
00840682138161 EUDAMEDFDA UDI
Basic UDI-DI
B-00840682138161 EUDAMED
FDA Product Code
CAP FDA UDI
CCK FDA UDI
CBR FDA UDI
BZL FDA UDI
NHP FDA UDI
CCL FDA UDI
CBS FDA UDI
NHO FDA UDI
NHQ FDA UDI
CBQ FDA UDI
BZK FDA UDI
EMDN Code
Z1203020285 MULTI-PARAMETER MONITORS - CONSUMABLES EUDAMED
GMDN Term
Gas-sampling/monitoring respiratory tubing, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
868.2600 FDA UDI
868.1400 FDA UDI
868.1700 FDA UDI
868.1730 FDA UDI
868.1500 FDA UDI
868.1720 FDA UDI
868.1620 FDA UDI
868.1850 FDA UDI
Market of Registration
Finland 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

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

Category: General-purpose multi-parameter bedside monitor

D-lite++ Patient Spirometry Set, 2 m/7 ft by GE Healthcare Finland Oy — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose multi-parameter bedside monitor.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
FI-MF-000001176

Sources (2)

  • EUDAMED 0509eacf-3eda-4d58-b49b-06e5cb2cd155 61 fields · synced Oct 8, 2026
  • FDA UDI 87eade2c-0071-4c3f-8fe9-99fdbd9dae4f 33 fields · synced May 30, 2026