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24PW - Maryland SBK

FDA UDI

Class I (US FDA UDI)

by Certified Safety Manufacturing, Inc.

Identity

Trade Name
24PW - Maryland SBK FDA UDI
Generic Name
Non-rebreathing valve, single-use FDA UDI
Device Name
24PW - Maryland SBK FDA UDI
Model / Reference
S202-154 FDA UDI
Description
24PW - Maryland SBK FDA UDI

Identifiers

Catalog Number
S202-154 FDA UDI
Primary DI / UDI-DI
00766588021546 FDA UDI
FDA Product Code
KGX FDA UDI
EFQ FDA UDI
HMP FDA UDI
LRR FDA UDI
CBP FDA UDI
GMDN Term
Non-rebreathing valve, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5240 FDA UDI
878.4440 FDA UDI
868.5870 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: First aid kit, medicatedAdhesive bandageNon-woven gauze padDressing-fixation skin adhesive tape, non-silicone

24PW - Maryland SBK by Certified Safety Manufacturing, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Eye pad.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d99e7ef8-9e6f-4ca3-bcee-23df7008cd40 35 fields · synced May 30, 2026