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Mark III MIL Resuscitatorwith butyl rubber outer cover and Mark III pa

FDA UDI

Class II (US FDA UDI)

by Ambu A/S

Identity

Trade Name
Mark III MIL Resuscitatorwith butyl rubber outer cover and Mark III pa FDA UDI
Generic Name
Pulmonary resuscitator, manual, reusable FDA UDI
Device Name
Ambu Mark III (Mil) resuscitator with butyl outer cover, complete with Ambu Mark III patient valve, transparent face mask size 5, special hanging strap with snap hook and gas filter adapter (filter thread 2.342in x 8 threads/in.), supplied in pouch & carton FDA UDI
Model / Reference
A233006000 FDA UDI
Description
Ambu Mark III (Mil) resuscitator with butyl outer cover, complete with Ambu Mark III patient valve, transparent face mask size 5, special hanging strap with snap hook and gas filter adapter (filter thread 2.342in x 8 threads/in.), supplied in pouch & carton FDA UDI

Identifiers

Catalog Number
A233006000 FDA UDI
Primary DI / UDI-DI
05707480031054 FDA UDI
FDA Product Code
BTM FDA UDI
GMDN Term
Pulmonary resuscitator, manual, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5915 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Mark III MIL Resuscitatorwith butyl rubber outer cover and Mark III pa by Ambu A/S — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ambu A/S

Sources (1)

  • FDA UDI 18334da9-4b9c-4065-8bd4-cc9cd2ba89c4 37 fields · synced Jun 8, 2026