← Back to catalogue

PQ Pouches 3 1/2 x 10"(200) Blue

FDA UDI

Class II (US FDA UDI)

by Pearson Dental Supplies, Inc.

Identity

Trade Name
PQ Pouches 3 1/2 x 10"(200) Blue FDA UDI
Generic Name
Sterilization packaging, single-use FDA UDI
Device Name
Pk. of 200 FDA UDI
Model / Reference
P23-0915 FDA UDI
Description
Pk. of 200 FDA UDI

Identifiers

Primary DI / UDI-DI
D724P2309151 FDA UDI
FDA Product Code
FRC FDA UDI
GMDN Term
Sterilization packaging, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.2800 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

Yes

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

PQ Pouches 3 1/2 x 10"(200) Blue by Pearson Dental Supplies, 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

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

Manufacturer

Sources (1)

  • FDA UDI ce4bab9b-6737-4415-94d5-09986484d93d 33 fields · synced May 30, 2026