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Lugols

FDA UDI

Class I (US FDA UDI)

by Premier Dental Products Company

Identity

Trade Name
Lugols FDA UDI
Generic Name
Endoscopy mucosal lesion stain FDA UDI
Device Name
Lugol’s Solution, 8ml bottles with applicators- 12 pack FDA UDI
Model / Reference
9045056 FDA UDI
Description
Lugol’s Solution, 8ml bottles with applicators- 12 pack FDA UDI

Identifiers

Primary DI / UDI-DI
00348783001242 FDA UDI
FDA Product Code
IAM FDA UDI
GMDN Term
Endoscopy mucosal lesion stain FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.4010 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Endoscopy mucosal lesion stain

Lugols by Premier Dental Products Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopy mucosal lesion stain.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 72757169-f252-46a4-ac1a-3a125a68611e 33 fields · synced May 30, 2026