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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
Single-lumen haemodialysis catheter, peripheral vascular FDA UDI
Device Name
Frontal Sinus Forceps, 45 Degrees Vertical, 2mm Cups, Shaft Length 140mm, Overall Length 8.9" (225mm) FDA UDI
Model / Reference
114-7611-F FDA UDI
Description
Frontal Sinus Forceps, 45 Degrees Vertical, 2mm Cups, Shaft Length 140mm, Overall Length 8.9" (225mm) FDA UDI

Identifiers

Primary DI / UDI-DI
00194613068912 FDA UDI
FDA Product Code
LRC FDA UDI
GMDN Term
Single-lumen haemodialysis catheter, peripheral vascular FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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: Single-lumen haemodialysis catheter, peripheral vascular

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 Single-lumen haemodialysis catheter, peripheral vascular.

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 157e20e6-c36f-4351-803b-cfb22dd308ac 34 fields · synced Jun 8, 2026