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Ellman Cots

FDA UDI

Class I (US FDA UDI)

by Cynosure, LLC

Identity

Trade Name
Ellman Cots FDA UDI
Generic Name
Finger/toe tourniquet, non-sterile FDA UDI
Device Name
COTS - DIGIT TOURNIQUET 4 EA. S, M, L FDA UDI
Model / Reference
ECOTS FDA UDI
Description
COTS - DIGIT TOURNIQUET 4 EA. S, M, L FDA UDI

Identifiers

Catalog Number
ECOTS FDA UDI
Primary DI / UDI-DI
00841494107031 FDA UDI
FDA Product Code
OJS FDA UDI
GMDN Term
Finger/toe tourniquet, non-sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.5900 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

Yes

FDA UDI

Category: Finger/toe tourniquet, non-sterile

Ellman Cots by Cynosure, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Finger/toe tourniquet, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cynosure, LLC

Sources (1)

  • FDA UDI 1e7fdb6d-6e56-4bbe-80d0-4b0bd2b3cc42 34 fields · synced May 30, 2026