Trinity Sterile, Inc.

FDA UDI

by Trinity Sterile, Inc.

Identity

Trade Name: Trinity Sterile, Inc. FDA UDI
Generic Name: Wound dressing kit, non-medicated FDA UDI
Device Name: PEDI/ADULT DRESS CHNG KIT FDA UDI
Model / Reference: 81543 FDA UDI
Description: PEDI/ADULT DRESS CHNG KIT FDA UDI

Identifiers

Primary DI / UDI-DI: 10841767106706 FDA UDI
GMDN Term: Wound dressing kit, non-medicated FDA UDI

Classification

Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

Yes

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Ethylene Oxide FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Wound dressing kit, non-medicated

Trinity Sterile, Inc. by Trinity Sterile, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	N/A	Pending data

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Manufacturer

Manufacturer: Trinity Sterile, Inc.

Sources (1)

FDA UDI ecbe0aaf-c39e-47b1-a50b-e3498ee58ca1 33 fields · synced May 31, 2026