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Therapy Mask 3100

FDA UDI

Class II (US FDA UDI)

by Respironics, Inc.

Identity

Trade Name
Therapy Mask 3100 FDA UDI
Generic Name
CPAP/BPAP nasal mask, reusable FDA UDI
Model / Reference
Large, Therapy Mask 3100 Silicone Pillow FDA UDI

Identifiers

Catalog Number
1145058 FDA UDI
Primary DI / UDI-DI
00606959060128 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

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: CPAP/BPAP nasal mask, reusable

Therapy Mask 3100 by Respironics, Inc. — 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
Respironics, Inc.

Sources (1)

  • FDA UDI b0d65338-6f28-4b2a-bdc7-f33116d6b849 34 fields · synced Jun 6, 2026