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Prima 450 Anaesthetic Machine

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 5011303

by Penlon Limited

Identity

Trade Name
Prima 450 Anaesthetic Machine EUDAMED
Penlon FDA UDI
Generic Name
Anaesthesia unit, mobile FDA UDI
Device Name
Prima 450 Anaesthetic Machine EUDAMED
Model / Reference
5011303 EUDAMED
Prima 450 FDA UDI

Identifiers

Primary DI / UDI-DI
05051977000000 EUDAMEDFDA UDI
Basic UDI-DI
B-05051977000000 EUDAMED
510(k) Number
K061102 FDA UDI
FDA Product Code
BSZ FDA UDI
EMDN Code
Z1203010101 ANAESTHESIA DEVICES EUDAMED
GMDN Term
Anaesthesia unit, mobile FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
868.5160 FDA UDI
Market of Registration
Poland 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

Prima 450 Anaesthetic Machine 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 a438ef02-a074-4480-ad90-4b8abc971b47 61 fields · synced Jun 18, 2026
  • FDA UDI 23dc4670-6032-441f-a0bc-1eda3abf9447 34 fields · synced May 30, 2026