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Sigma Delta Vaporizer / Halothane

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 410502H Model Sigma Delta

by Penlon Limited

Identity

Trade Name
Sigma Delta Vaporizer / Halothane EUDAMED
Penlon FDA UDI
Generic Name
Halothane anaesthesia vaporizer FDA UDI
Device Name
Halothane Anaesthesia Vaporizer EUDAMED
Sigma Delta Vaporizer / Halothane FDA UDI
Model / Reference
Sigma Delta EUDAMED
410502H EUDAMED
Sigma Delta Vaporizer / Halothane FDA UDI
Description
Sigma Delta Vaporizer / Halothane FDA UDI

Identifiers

Catalog Number
410502H FDA UDI
Primary DI / UDI-DI
05051977001465 EUDAMEDFDA UDI
Basic UDI-DI
B-05051977001465 EUDAMED
510(k) Number
K002343 FDA UDI
FDA Product Code
CAD FDA UDI
EMDN Code
Z1203010180 ANAESTHESIA SYSTEMS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Halothane anaesthesia vaporizer FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
868.5880 FDA UDI
Market of Registration
Belgium EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

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

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sigma Delta Vaporizer / Halothane by Penlon Limited — Class IIb — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Penlon Limited
EUDAMED SRN
GB-MF-000025115
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (2)

  • EUDAMED 1e481503-4820-4bbe-bd84-c96a65b0f5f6 61 fields · synced Jun 18, 2026
  • FDA UDI 0dd78b81-f6fa-4f72-8629-a159678dd7a7 36 fields · synced May 30, 2026