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Tc-100

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
TC-100 FDA UDI
Generic Name
Orthopaedic osteotome blade, reusable FDA UDI
Device Name
CANN OSTEO BLADE PLATE 4 HOLE INFANT 25MM FDA UDI
Model / Reference
71925281 FDA UDI
Description
CANN OSTEO BLADE PLATE 4 HOLE INFANT 25MM FDA UDI

Identifiers

Catalog Number
71925281 FDA UDI
Primary DI / UDI-DI
00885556043516 FDA UDI
FDA Product Code
KTT FDA UDI
GMDN Term
Orthopaedic osteotome blade, reusable 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthopaedic osteotome blade, reusable

Tc-100 by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic osteotome blade, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 999d12ce-a974-4046-8e04-b71b3bf2d08f 35 fields · synced Jun 8, 2026