Clamp T Handle (Black) with 5/32 tool shaft

FDA UDI

Class II (US FDA UDI)

by Medshape, Inc.

Identity

Trade Name: Clamp T Handle (Black) with 5/32 tool shaft FDA UDI
Generic Name: Orthopaedic fixation plate, non-bioabsorbable FDA UDI
Model / Reference: DNE-9000-TH-532 FDA UDI

Identifiers

Primary DI / UDI-DI: 00850062461734 FDA UDI
FDA Product Code: KTT FDA UDI
GMDN Term: Orthopaedic fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3030 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic fixation plate, non-bioabsorbable

Clamp T Handle (Black) with 5/32 tool shaft by Medshape, Inc. — Class II — 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	Class II	Pending data

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Manufacturer

Manufacturer: Medshape, Inc.

Sources (1)

FDA UDI 9b4068c6-70f4-44b4-b373-e8408c6ff44f 32 fields · synced May 31, 2026