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Steinmann Pin Set

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
STEINMANN PIN SET FDA UDI
Generic Name
Orthopaedic trocar blade, reusable FDA UDI
Device Name
STEINMANN PIN SET DELUXE DOUBLE ENDED TIPS FDA UDI
Model / Reference
1106-730 FDA UDI
Description
STEINMANN PIN SET DELUXE DOUBLE ENDED TIPS FDA UDI

Identifiers

Catalog Number
1106-730 FDA UDI
Primary DI / UDI-DI
00192896097834 FDA UDI
510(k) Number
K100736 FDA UDI
FDA Product Code
HTY FDA UDI
GMDN Term
Orthopaedic trocar blade, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthopaedic trocar blade, reusable

Steinmann Pin Set by Sontec Instruments, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic trocar blade, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 926c4974-5b24-416c-a456-447fd4718433 36 fields · synced Jun 1, 2026