← Back to catalogue

Customed

FDA UDI

Class II (US FDA UDI)

by Customed, Inc.

Identity

Trade Name
CUSTOMED FDA UDI
Generic Name
Nebulizing system delivery set, single-use FDA UDI
Device Name
NEBULIZER SET 6CC (ML) W/ADULT MASK AND STANDARD CONNECTOR FDA UDI
Model / Reference
712057143105 FDA UDI
Description
NEBULIZER SET 6CC (ML) W/ADULT MASK AND STANDARD CONNECTOR FDA UDI

Identifiers

Catalog Number
9003105 FDA UDI
Primary DI / UDI-DI
M20890031050 FDA UDI
510(k) Number
K091272 FDA UDI
FDA Product Code
CAF FDA UDI
GMDN Term
Nebulizing system delivery set, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5630 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Total Volume — 6 Milliliter FDA UDI

Category: Nebulizing system delivery set, single-use

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

Similar devices

Also classified as Nebulizing system delivery set, single-use.

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

Manufacturer
Customed, Inc.

Sources (1)

  • FDA UDI 0a90df31-45e1-4652-b553-2b151ee2fe45 38 fields · synced Jun 8, 2026