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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Pulmonary function testing filter/mouthpiece FDA UDI
Device Name
FILTER,PULMONARY,FUNCTION,ELLIPTICAL,BLU FDA UDI
Model / Reference
DYNJ760ELB FDA UDI
Description
FILTER,PULMONARY,FUNCTION,ELLIPTICAL,BLU FDA UDI

Identifiers

Catalog Number
DYNJ760ELB FDA UDI
Primary DI / UDI-DI
10888277652460 FDA UDI
510(k) Number
K042758 FDA UDI
FDA Product Code
BZG FDA UDI
GMDN Term
Pulmonary function testing filter/mouthpiece FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1840 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

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: Pulmonary function testing filter/mouthpiece

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

Similar devices

Also classified as Pulmonary function testing filter/mouthpiece.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2d8dbf41-6e7f-4d23-ac34-2804e0481c65 36 fields · synced May 30, 2026