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Sizer For Lacrijet

FDA UDI

Class I (US FDA UDI)

by Fci S A S Fci 20 22

Identity

Trade Name
SIZER FOR LACRIJET FDA UDI
Generic Name
Surgical depth gauge, single-use FDA UDI
Device Name
SIZER FOR LACRIJET FDA UDI
Model / Reference
S1.1288 FDA UDI
Description
SIZER FOR LACRIJET FDA UDI

Identifiers

Primary DI / UDI-DI
03700773723287 FDA UDI
FDA Product Code
HNL FDA UDI
GMDN Term
Surgical depth gauge, single-use 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

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical depth gauge, single-use

Sizer For Lacrijet by Fci S A S Fci 20 22 — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical depth gauge, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fci S A S Fci 20 22

Sources (1)

  • FDA UDI 5dbd990e-5bab-40f3-822d-0d13cdd7c6eb 33 fields · synced May 30, 2026