← Back to catalogue

Bausch + Lomb

FDA UDI

Class I (US FDA UDI)

by Bausch & Lomb Incorporated

Identity

Trade Name
Bausch + Lomb FDA UDI
Generic Name
Tape measure, reusable FDA UDI
Device Name
RULE SS STEEL FLEX 6IN X 1/2IN FDA UDI
Model / Reference
E2420 FDA UDI
Description
RULE SS STEEL FLEX 6IN X 1/2IN FDA UDI

Identifiers

Catalog Number
E2420 FDA UDI
Primary DI / UDI-DI
00757770460250 FDA UDI
FDA Product Code
FTY FDA UDI
GMDN Term
Tape measure, 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: Tape measure, reusable

Bausch + Lomb by Bausch & Lomb Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tape measure, 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
Bausch & Lomb Incorporated

Sources (1)

  • FDA UDI f92fbb03-11a5-4d41-9fc7-883cda3a71e9 34 fields · synced Jun 8, 2026