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Mabis

FDA UDI

Class II (US FDA UDI)

by Dms Holdings, Inc.,

Identity

Trade Name
MABIS FDA UDI
Generic Name
Nebulizing system delivery set, reusable FDA UDI
Device Name
NEBULIZER ONLY FOR ALL MABIS COMPRESSOR NEBS FDA UDI
Model / Reference
40-101-000 FDA UDI
Description
NEBULIZER ONLY FOR ALL MABIS COMPRESSOR NEBS FDA UDI

Identifiers

Catalog Number
40-101-000 FDA UDI
Primary DI / UDI-DI
00767056401013 FDA UDI
510(k) Number
K031413 FDA UDI
FDA Product Code
CAF FDA UDI
GMDN Term
Nebulizing system delivery set, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5630 FDA UDI
Commercial Distribution
Not 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

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

No

FDA UDI

Mabis by Dms Holdings, Inc., — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dms Holdings, Inc.,

Sources (1)

  • FDA UDI 71b499c5-bbc5-4335-9410-b6462cede3ea 36 fields · synced May 30, 2026