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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
Flexible endoscopic tissue manipulation forceps, reusable FDA UDI
Device Name
Double Action Biopsy Cup Forcep Working Length 5 1/8" (130mm) Cup Size 2mm x 4mm 45 Degree Bend Jaw Opens Vertically With Leur Lock FDA UDI
Model / Reference
232-I42-49-LL FDA UDI
Description
Double Action Biopsy Cup Forcep Working Length 5 1/8" (130mm) Cup Size 2mm x 4mm 45 Degree Bend Jaw Opens Vertically With Leur Lock FDA UDI

Identifiers

Primary DI / UDI-DI
00194613081829 FDA UDI
FDA Product Code
FCL FDA UDI
GMDN Term
Flexible endoscopic tissue manipulation forceps, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.1075 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: Flexible endoscopic tissue manipulation forceps, 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 Flexible endoscopic tissue manipulation forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Med Saver, Inc.

Sources (1)

  • FDA UDI 7f678b8c-a2f2-4605-ad3f-b3ac267dd2e6 34 fields · synced May 30, 2026