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Ryder Micro Needle Holder

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
RYDER MICRO NEEDLE HOLDER FDA UDI
Generic Name
Suturing needle holder, reusable FDA UDI
Device Name
RYDER MICRO NEEDLE HOLDER DELICATE TUNGSTEN CARBIDE SERRATED TIP FDA UDI
Model / Reference
1100-122 FDA UDI
Description
RYDER MICRO NEEDLE HOLDER DELICATE TUNGSTEN CARBIDE SERRATED TIP FDA UDI

Identifiers

Catalog Number
1100-122 FDA UDI
Primary DI / UDI-DI
00192896081192 FDA UDI
FDA Product Code
FHQ FDA UDI
GMDN Term
Suturing needle holder, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.4730 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

Yes

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 — 5 Inch FDA UDI

Category: Suturing needle holder, reusable

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

Similar devices

Also classified as Suturing needle holder, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7e307438-0b78-4647-8b0a-d82850b650b3 36 fields · synced May 31, 2026