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75V - Class A Select - 3 Shelf Cabinet

FDA UDI

Class II (US FDA UDI)

by Certified Safety Manufacturing, Inc.

Identity

Trade Name
75V - Class A Select - 3 Shelf Cabinet FDA UDI
Generic Name
Non-woven gauze pad FDA UDI
Device Name
75V - Class A Select - 3 Shelf Cabinet FDA UDI
Model / Reference
K618-036 FDA UDI
Description
75V - Class A Select - 3 Shelf Cabinet FDA UDI

Identifiers

Catalog Number
K618-036 FDA UDI
Primary DI / UDI-DI
00766588180366 FDA UDI
FDA Product Code
CBP FDA UDI
LRR FDA UDI
EFQ FDA UDI
KGX FDA UDI
HMP FDA UDI
IMD FDA UDI
GMDN Term
Non-woven gauze pad FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5870 FDA UDI
880.5240 FDA UDI
878.4440 FDA UDI
890.5710 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 padWound-nonadherent dressing, absorbent, non-antimicrobial

75V - Class A Select - 3 Shelf Cabinet by Certified Safety Manufacturing, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental suction system rinsing unit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Certified Safety Manufacturing, Inc.

Sources (1)

  • FDA UDI 8d446efe-348c-4173-8519-6325d8af6ddb 35 fields · synced May 29, 2026