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Endocator

FDA UDI

Class I (US FDA UDI)

by Endo Direct, Llc

Identity

Trade Name
Endocator FDA UDI
Generic Name
Light meter FDA UDI
Model / Reference
ENDOCATOR FDA UDI

Identifiers

Primary DI / UDI-DI
10810138822705 FDA UDI
FDA Product Code
JJQ FDA UDI
GMDN Term
Light meter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2300 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Light meter

Endocator by Endo Direct, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Endo Direct, Llc

Sources (1)

  • FDA UDI 056c6b30-1596-4829-b50b-04486f5aab2e 32 fields · synced May 30, 2026