← Back to catalogue

Mask ClassicStar Nasal NV, S

FDA UDI

Class II (US FDA UDI)

by Drägerwerk AG & Co. KGaA

Identity

Trade Name
Mask ClassicStar Nasal NV, S FDA UDI
Generic Name
Rebreathing oxygen face mask FDA UDI
Model / Reference
MP01623 FDA UDI

Identifiers

Primary DI / UDI-DI
04048675250821 FDA UDI
510(k) Number
K081743 FDA UDI
FDA Product Code
CBK FDA UDI
GMDN Term
Rebreathing oxygen face mask FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5895 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

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Rebreathing oxygen face mask

Mask ClassicStar Nasal NV, S by Drägerwerk AG & Co. KGaA — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rebreathing oxygen face mask.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 62a8e16e-261a-44ce-9270-ed177e7ebe15 34 fields · synced May 30, 2026