Debakey Needle Pulling Forceps

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name: Debakey Needle Pulling Forceps FDA UDI
Generic Name: Suturing unit, reusable FDA UDI
Device Name: Debakey Needle Pulling Forceps With Guide Pin Tungsten Carbide Serrated 3.5 Millimeter Tip FDA UDI
Model / Reference: 2200-090P FDA UDI
Description: Debakey Needle Pulling Forceps With Guide Pin Tungsten Carbide Serrated 3.5 Millimeter Tip FDA UDI

Identifiers

Catalog Number: 2200-090P FDA UDI
Primary DI / UDI-DI: 00192896121201 FDA UDI
FDA Product Code: HTD FDA UDI
GMDN Term: Suturing unit, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Dry Heat Sterilization FDA UDI

Dimensions & Sizes

Size: Length — 9.5 Inch FDA UDI

Category: Suturing unit, reusable

Debakey Needle Pulling Forceps by Sontec Instruments, Inc. — Class I — 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 I	Pending data

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Manufacturer

Manufacturer: Sontec Instruments, Inc.

Sources (1)

FDA UDI 8bf3e3c7-ad22-45bb-afd8-ffa83de3c96f 36 fields · synced May 30, 2026