McKesson

FDA UDI

Class II (US FDA UDI)

by Mckesson Medical-Surgical Inc.

Identity

Trade Name: McKesson FDA UDI
Generic Name: Uterine tenaculum FDA UDI
Device Name: FORCEP, SCHROEDER TEN SG STRT FDA UDI
Model / Reference: 43-1-386 FDA UDI
Description: FORCEP, SCHROEDER TEN SG STRT FDA UDI

Identifiers

Primary DI / UDI-DI: 10612479141961 FDA UDI
FDA Product Code: HDC FDA UDI
GMDN Term: Uterine tenaculum FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 884.4530 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

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Implantable

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Contains Latex

FDA UDI

Prescription Use

Yes

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Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

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Lot / Batch Number

Yes

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Serial Number

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Expiration Date

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Manufacturing Date

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Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Uterine tenaculum

This is a detailed description of the McKesson Forcep, Schroeder Ten SG STRT. A reusable hand-held surgical instrument used for grasping and manipulating uterine tissue during surgical interventions or examinations. It features a self-retaining design with stainless steel construction and has a variety of sizes available.

Similar devices

Also classified as Uterine tenaculum.

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GEN2 — SURGIX MEDICAL LLC · Class II
GEN2 — SURGIX MEDICAL LLC · Class II

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: Mckesson Medical-Surgical Inc.

Sources (1)

FDA UDI fee512b7-39b5-403e-ae78-e3cb9668c383 33 fields · synced Jul 12, 2026