← Back to catalogue

Tech-Med

FDA UDI

Class I (US FDA UDI)

by Dukal LLC

Identity

Trade Name
Tech-Med FDA UDI
Generic Name
Tape measure, single-use FDA UDI
Device Name
Paper Tape Measure 36" FDA UDI
Model / Reference
4412 FDA UDI
Description
Paper Tape Measure 36" FDA UDI

Identifiers

Catalog Number
4412 FDA UDI
Primary DI / UDI-DI
10665973022427 FDA UDI
FDA Product Code
FTY FDA UDI
GMDN Term
Tape measure, single-use 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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

Category: Tape measure, single-use

Tech-Med by Dukal LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tape measure, single-use.

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
Dukal LLC

Sources (1)

  • FDA UDI ce5e2c50-9f3c-4ca0-b5f9-8259ad7366e8 35 fields · synced Jun 1, 2026