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Siesta Nasal Mask (without Headgear)-L

FDA UDI

Class II (US FDA UDI)

by Bmc Medical., Ltd.

Identity

Trade Name
Siesta Nasal Mask (without Headgear)-L FDA UDI
Generic Name
CPAP/BPAP nasal mask, reusable FDA UDI
Device Name
Siesta Nasal Mask (without Headgear)-L FDA UDI
Model / Reference
N5B(Large) FDA UDI
Description
Siesta Nasal Mask (without Headgear)-L FDA UDI

Identifiers

Primary DI / UDI-DI
06948538364093 FDA UDI
FDA Product Code
BZD FDA UDI
GMDN Term
CPAP/BPAP nasal mask, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5905 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: CPAP/BPAP nasal mask, reusable

Siesta Nasal Mask (without Headgear)-L by Bmc Medical., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as CPAP/BPAP nasal mask, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bmc Medical., Ltd.

Sources (1)

  • FDA UDI a67c7cb3-5b60-40db-87f5-513c61581e98 33 fields · synced May 30, 2026