Medline/MMS Sales

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name: Medline/MMS Sales FDA UDI
Generic Name: Non-rebreathing valve, single-use FDA UDI
Device Name: FILTER-ANESTHESIA,BULK FDA UDI
Model / Reference: 75-2001 FDA UDI
Description: FILTER-ANESTHESIA,BULK FDA UDI

Identifiers

Catalog Number: 75-2001 FDA UDI
Primary DI / UDI-DI: 10884389045039 FDA UDI
510(k) Number: K925217 FDA UDI
FDA Product Code: CAH FDA UDI
GMDN Term: Non-rebreathing valve, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5260 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Non-rebreathing valve, single-use

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

Similar devices

Also classified as Non-rebreathing valve, single-use.

16PW - Class A Burn Relief — Certified Safety Manufacturing, Inc. · Class I
16PW - Class A Blue Metal Detectable - Poly White — Certified Safety Manufacturing, Inc. · U
EMT - Class B Trauma - Bag — Certified Safety Manufacturing, Inc. · Class I
810X - CPRotector® - w/Nitrile Gloves - 2/Unit — Certified Safety Manufacturing, Inc. · Class II
Curaplex — BOUND TREE MEDICAL, LLC · Class I
36M - Class B Select - Metal — Certified Safety Manufacturing, Inc. · Class I
10PW - Oklahoma Gas & Electric - Poly White — Certified Safety Manufacturing, Inc. · N
EMT - Duke Energy TD - Red Bag — Certified Safety Manufacturing, Inc. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Medline Industries, Inc.

Sources (1)

FDA UDI 16072629-7dca-4240-8330-49261dcf35d5 36 fields · synced May 29, 2026

Medline/MMS Sales

Identity

Identifiers

Classification

Clinical & Handling

Similar devices

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

Manufacturer

Sources (1)