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Rumex

FDA UDI

Class I (US FDA UDI)

by Rumex International Co.

Identity

Trade Name
Rumex FDA UDI
Generic Name
LASEK alcohol well, reusable FDA UDI
Device Name
Tunnel Maker, 4.40/5.60 mm Diameter, 0.30 mm Width, Left, Stainless Steel FDA UDI
Model / Reference
16-173S FDA UDI
Description
Tunnel Maker, 4.40/5.60 mm Diameter, 0.30 mm Width, Left, Stainless Steel FDA UDI

Identifiers

Catalog Number
16-173S FDA UDI
Primary DI / UDI-DI
00840159907863 FDA UDI
FDA Product Code
HRH FDA UDI
GMDN Term
LASEK alcohol well, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: LASEK alcohol well, reusable

Rumex by Rumex International Co. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as LASEK alcohol well, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Rumex International Co.

Sources (1)

  • FDA UDI 65a0ce46-d035-4172-a906-8c1b61d88c89 34 fields · synced Jun 9, 2026