← 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
Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
Device Name
Jones Inamura Capsulorhexis Forceps, Curved, E-Range, Cross-Action Tips, 1.5mm Width At Pivot Box, Incision Down To 1.8mm, Pointed Serrated Interlocking Tips, Tip To Pivot Point 11mm, Marks On Shaft Every 1mm From Tip To 6mm, Tips Angled 45 Degrees To Handle, Flat Handle, Overall Length 4-1/2" (115mm) FDA UDI
Model / Reference
2-716G-10E FDA UDI
Description
Jones Inamura Capsulorhexis Forceps, Curved, E-Range, Cross-Action Tips, 1.5mm Width At Pivot Box, Incision Down To 1.8mm, Pointed Serrated Interlocking Tips, Tip To Pivot Point 11mm, Marks On Shaft Every 1mm From Tip To 6mm, Tips Angled 45 Degrees To Handle, Flat Handle, Overall Length 4-1/2" (115mm) FDA UDI

Identifiers

Primary DI / UDI-DI
00194613085162 FDA UDI
FDA Product Code
HNR FDA UDI
GMDN Term
Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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: Ophthalmic soft-tissue manipulation forceps, tweezers-like, 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 Ophthalmic soft-tissue manipulation forceps, tweezers-like, 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 0c58ac40-5e22-4714-94f4-9207aeb4f3b6 34 fields · synced Jun 6, 2026