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Tri-Tech Forensics, Inc.

FDA UDI

Class II (US FDA UDI)

by Tri-Tech Forensics Inc.

Identity

Trade Name
Tri-Tech Forensics, Inc. FDA UDI
Generic Name
Victim sexual-assault forensic evidence kit FDA UDI
Device Name
Tri-Tech Forensics Custom Sexual Assault Kit FDA UDI
Model / Reference
RE-1MS FDA UDI
Description
Tri-Tech Forensics Custom Sexual Assault Kit FDA UDI

Identifiers

Primary DI / UDI-DI
00869373000242 FDA UDI
510(k) Number
K922343 FDA UDI
FDA Product Code
JKA FDA UDI
GMDN Term
Victim sexual-assault forensic evidence kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1675 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Height — 2.375 Inch FDA UDI
Width — 6.75 Inch FDA UDI
Length — 10.25 Inch FDA UDI

Category: Victim sexual-assault forensic evidence kit

Tri-Tech Forensics, Inc. by Tri-Tech Forensics Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tri-Tech Forensics Inc.

Sources (1)

  • FDA UDI 27b3e5cc-3d71-41a9-975a-821f6e5f8109 35 fields · synced Jun 6, 2026