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Mapleson Anesthesia Breathing Circuit

FDA UDI

Class I (US FDA UDI)

by Mercury Enterprises, Inc.

Identity

Trade Name
Mapleson Anesthesia Breathing Circuit FDA UDI
Generic Name
Anaesthesia breathing circuit, single-use FDA UDI
Model / Reference
10-80381 FDA UDI

Identifiers

Primary DI / UDI-DI
10641043803813 FDA UDI
FDA Product Code
CAI FDA UDI
GMDN Term
Anaesthesia breathing circuit, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5240 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Anaesthesia breathing circuit, single-use

Mapleson Anesthesia Breathing Circuit by Mercury Enterprises, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anaesthesia breathing circuit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d4c44414-1c25-41eb-8d3a-2dab6cfc9b7d 33 fields · synced Jun 8, 2026