← Back to catalogue

TripleCheck™ Pouch

FDA UDI

Class II (US FDA UDI)

by Safco Dental Supply

Identity

Trade Name
TripleCheck™ Pouch FDA UDI
Generic Name
Sterilization packaging, single-use FDA UDI
Device Name
SAFCO STERILIZATION POUCH 2.25 X 4 FDA UDI
Model / Reference
102-0181 FDA UDI
Description
SAFCO STERILIZATION POUCH 2.25 X 4 FDA UDI

Identifiers

Catalog Number
102-0181 FDA UDI
Primary DI / UDI-DI
D72310201813 FDA UDI
FDA Product Code
KCT FDA UDI
GMDN Term
Sterilization packaging, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6850 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

Yes

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: Sterilization packaging, single-use

TripleCheck™ Pouch by Safco Dental Supply — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sterilization packaging, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Safco Dental Supply

Sources (1)

  • FDA UDI 22477cf6-d698-4e21-b5e0-42e65061fb55 36 fields · synced May 31, 2026