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SPUR® II Pediatric ResuscitatorSingle Patient Use Resuscitator

FDA UDI

Class II (US FDA UDI)

by Ambu A/S

Identity

Trade Name
SPUR® II Pediatric ResuscitatorSingle Patient Use Resuscitator FDA UDI
Generic Name
Pulmonary resuscitator, manual, single-use FDA UDI
Device Name
Ambu SPUR II Pediatric with open reservoir 40, with Duraclear face mask size neonate, infant, toddler/pediatric, small adult and medium adult and with pressure line adapter. 6 pcs/box FDA UDI
Model / Reference
531614026 FDA UDI
Description
Ambu SPUR II Pediatric with open reservoir 40, with Duraclear face mask size neonate, infant, toddler/pediatric, small adult and medium adult and with pressure line adapter. 6 pcs/box FDA UDI

Identifiers

Catalog Number
531614026 FDA UDI
Primary DI / UDI-DI
05707480033782 FDA UDI
FDA Product Code
BTM FDA UDI
GMDN Term
Pulmonary resuscitator, manual, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5915 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

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

Category: Pulmonary resuscitator, manual, single-use

SPUR® II Pediatric ResuscitatorSingle Patient Use Resuscitator by Ambu A/S — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pulmonary resuscitator, manual, single-use.

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 b6617b7f-f82f-4729-929c-04a596c16dbf 38 fields · synced May 31, 2026