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Ethox

FDA UDI

Class I (US FDA UDI)

by Ethox Medical, Llc

Identity

Trade Name
Ethox FDA UDI
Generic Name
Surgical instrument interim-placement holder, single-use FDA UDI
Device Name
ETHOX SK-650N SURG 10 POCKET W/TAPE - NS FDA UDI
Model / Reference
950089600 FDA UDI
Description
ETHOX SK-650N SURG 10 POCKET W/TAPE - NS FDA UDI

Identifiers

Catalog Number
950089600 FDA UDI
Primary DI / UDI-DI
20889483149772 FDA UDI
FDA Product Code
KDD FDA UDI
GMDN Term
Surgical instrument interim-placement holder, 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Width — 5 Centimeter FDA UDI

Category: Surgical instrument interim-placement holder, single-use

Ethox by Ethox Medical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument interim-placement holder, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ethox Medical, Llc

Sources (1)

  • FDA UDI 5da5260e-9608-4add-b775-4a8fb1c22282 36 fields · synced Jun 6, 2026