← Back to catalogue

MSI Precision Specialty Instruments

FDA UDI

Class I (US FDA UDI)

by Med Saver, Inc.

Identity

Trade Name
MSI Precision Specialty Instruments FDA UDI
Generic Name
Suturing needle, reusable FDA UDI
Device Name
Martin Uterine Suture Needle, 1/2 Circle Cuttinge Edge, Size 4 FDA UDI
Model / Reference
16-860-4 FDA UDI
Description
Martin Uterine Suture Needle, 1/2 Circle Cuttinge Edge, Size 4 FDA UDI

Identifiers

Primary DI / UDI-DI
00194613093488 FDA UDI
FDA Product Code
GDM FDA UDI
GMDN Term
Suturing needle, 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

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Suturing needle, reusable

MSI Precision Specialty Instruments by Med Saver, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suturing needle, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Med Saver, Inc.

Sources (1)

  • FDA UDI bc4b6871-8c2d-446d-9643-465c81e6b87d 34 fields · synced May 30, 2026