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Bionix, LLC

FDA UDI

Class I (US FDA UDI)

by Bionix, LLC

Identity

Trade Name
Bionix, LLC FDA UDI
Generic Name
Tattoo ink, dermal FDA UDI
Device Name
Sample: 18g Accu-Tatt® FDA UDI
Model / Reference
SP-23100 FDA UDI
Description
Sample: 18g Accu-Tatt® FDA UDI

Identifiers

Catalog Number
23100 FDA UDI
Primary DI / UDI-DI
00714646000002 FDA UDI
FDA Product Code
FZZ FDA UDI
GMDN Term
Tattoo ink, dermal FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4660 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Category: Tattoo ink, dermal

Bionix, LLC by Bionix, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tattoo ink, dermal.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bionix, LLC

Sources (1)

  • FDA UDI 66f95b1c-67c5-4477-8b35-0010e2ab2dca 35 fields · synced Jun 8, 2026