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Heartline Ryder Needle Holder

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
HEARTLINE RYDER NEEDLE HOLDER FDA UDI
Generic Name
Suturing needle holder, reusable FDA UDI
Device Name
HEARTLINE RYDER NEEDLE HOLDER WITH LOCK TUNGSTEN CARBIDE SHAFT SQUEEZE HANDLE FDA UDI
Model / Reference
2800-021 FDA UDI
Description
HEARTLINE RYDER NEEDLE HOLDER WITH LOCK TUNGSTEN CARBIDE SHAFT SQUEEZE HANDLE FDA UDI

Identifiers

Primary DI / UDI-DI
00192896006812 FDA UDI
510(k) Number
K152400 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Suturing needle holder, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

Dimensions & Sizes

Size
Length — 23.5 Centimeter FDA UDI

Category: Suturing needle holder, reusable

Heartline Ryder Needle Holder by Sontec Instruments, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suturing needle holder, 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 eed081ca-c4f5-4eb1-94ff-0f5e07f69d4a 36 fields · synced May 31, 2026