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DHP/Health-Tec Sterilization Pouches

FDA UDI

Class II (US FDA UDI)

by Dental Health Products Inc

Identity

Trade Name
DHP/Health-Tec Sterilization Pouches FDA UDI
Generic Name
Sterilization packaging, single-use FDA UDI
Device Name
Health-Tec Sterilization Pouches, 3.5" x 9" 200/box FDA UDI
Model / Reference
600-100062 FDA UDI
Description
Health-Tec Sterilization Pouches, 3.5" x 9" 200/box FDA UDI

Identifiers

Catalog Number
600-100062 FDA UDI
Primary DI / UDI-DI
D7736001000621 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

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

Yes

FDA UDI

Category: Sterilization packaging, single-use

DHP/Health-Tec Sterilization Pouches by Dental Health Products Inc — 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

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Manufacturer

Sources (1)

  • FDA UDI 88771d3d-2f87-4ce4-93fa-42bca1e2f5b0 36 fields · synced May 31, 2026