← 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
Tongue depressor, surgical FDA UDI
Device Name
Ring Blade #4, Left, 34mm x 85mm Blade, Groove In Blade For EndoTracheal Tubes Up To 37Fr, Overall Length 6.4" (160mm) FDA UDI
Model / Reference
114-8620-4L FDA UDI
Description
Ring Blade #4, Left, 34mm x 85mm Blade, Groove In Blade For EndoTracheal Tubes Up To 37Fr, Overall Length 6.4" (160mm) FDA UDI

Identifiers

Primary DI / UDI-DI
00194613049355 FDA UDI
FDA Product Code
KBL FDA UDI
GMDN Term
Tongue depressor, surgical 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: Tongue depressor, surgical

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 Tongue depressor, surgical.

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 1431eef8-e8c7-403b-8b25-592f5ddc1a31 34 fields · synced May 30, 2026