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Top Quality Manufacturing, Inc ™

FDA UDI

Class II (US FDA UDI)

by Top Quality Manufacturing, Inc.

Identity

Trade Name
Top Quality Manufacturing, Inc ™ FDA UDI
Generic Name
Sterilization packaging, single-use FDA UDI
Device Name
Sterilization Pouches See Through Self Sealing w/ Built-In Indicator Item # SP2-1015 200 Pouches Single Use FDA UDI
Model / Reference
See Through Self Sealing w/ Built-In Indicator FDA UDI
Description
Sterilization Pouches See Through Self Sealing w/ Built-In Indicator Item # SP2-1015 200 Pouches Single Use FDA UDI

Identifiers

Catalog Number
SP2-1015 FDA UDI
Primary DI / UDI-DI
TQ26SP210151 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Sterilization packaging, single-use

Top Quality Manufacturing, Inc ™ by Top Quality Manufacturing, 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 02d8edd2-a079-447c-88c4-3ba907522a6f 35 fields · synced May 30, 2026