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Resuscitation Unit P type

FDA UDI

Class II (US FDA UDI)

by Atom Medical Corp

Identity

Trade Name
Resuscitation Unit P type FDA UDI
Generic Name
Respiratory oxygen therapy system FDA UDI
Model / Reference
60994 FDA UDI

Identifiers

Catalog Number
60994 FDA UDI
Primary DI / UDI-DI
04942962609944 FDA UDI
FDA Product Code
BTL FDA UDI
GMDN Term
Respiratory oxygen therapy system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5925 FDA UDI
Commercial Distribution
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

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

Dimensions & Sizes

Size
Width — 200 Millimeter FDA UDI
Height — 370 Millimeter FDA UDI

Category: Respiratory oxygen therapy system

Resuscitation Unit P type by Atom Medical Corp — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Respiratory oxygen therapy system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Atom Medical Corp

Sources (1)

  • FDA UDI c4c8f4a0-59a9-49a5-82e1-1f39a0cae31e 36 fields · synced May 30, 2026