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24M - Tampa Electric Co.

FDA UDI

Class U (US FDA UDI)

by Certified Safety Manufacturing, Inc.

Identity

Trade Name
24M - Tampa Electric Co. FDA UDI
Generic Name
Non-rebreathing valve, single-use FDA UDI
Device Name
24M Tampa Electric Co. FDA UDI
Model / Reference
K201-349 FDA UDI
Description
24M Tampa Electric Co. FDA UDI

Identifiers

Catalog Number
K201-349 FDA UDI
Primary DI / UDI-DI
00766588013497 FDA UDI
FDA Product Code
EFQ FDA UDI
LRR FDA UDI
KGX FDA UDI
CBP FDA UDI
GMDN Term
Non-rebreathing valve, single-use FDA UDI

Classification

Device Class
U FDA UDI
Regulation Number
880.5240 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

24M - Tampa Electric Co. by Certified Safety Manufacturing, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-woven gauze roll/sheet.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0d40ac02-3489-435a-8b0d-79c68cca05da 35 fields · synced Jun 8, 2026