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Needleholder Positioner Insert

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
NEEDLEHOLDER POSITIONER INSERT FDA UDI
Generic Name
Suturing needle holder, reusable FDA UDI
Device Name
NEEDLEHOLDER POSITIONER WITH TUNGSTEN CARBIDE DUST CONVEX/CONCAVE SINGLE-ACTION JAW FOR TUBE SHAFT FDA UDI
Model / Reference
2901-324 FDA UDI
Description
NEEDLEHOLDER POSITIONER WITH TUNGSTEN CARBIDE DUST CONVEX/CONCAVE SINGLE-ACTION JAW FOR TUBE SHAFT FDA UDI

Identifiers

Primary DI / UDI-DI
B09929013240 FDA UDI
510(k) Number
K002877 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Suturing needle holder, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Commercial Distribution
Not 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

Dimensions & Sizes

Size
Length — 360 Millimeter FDA UDI

Needleholder Positioner Insert by Sontec Instruments, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 db176700-5db4-4794-a31f-1a49c4e11643 37 fields · synced Jun 1, 2026