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BlueBoost(TM) Submucosal Injectable Solution

FDA UDI

Class II (US FDA UDI)

by Micro-Tech (Nanjing) Co., Ltd.

Identity

Trade Name
BlueBoost(TM) Submucosal Injectable Solution FDA UDI
Generic Name
Injectable charcoal tattoo marker FDA UDI
Device Name
Product is sky-blue viscous liquid, the content is 10ml. Initial packaging is the syringe. FDA UDI
Model / Reference
SML10 FDA UDI
Description
Product is sky-blue viscous liquid, the content is 10ml. Initial packaging is the syringe. FDA UDI

Identifiers

Primary DI / UDI-DI
06932503562522 FDA UDI
510(k) Number
K200071 FDA UDI
FDA Product Code
PLL FDA UDI
GMDN Term
Injectable charcoal tattoo marker FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 10 Milliliter FDA UDI

Category: Injectable charcoal tattoo marker

BlueBoost(TM) Submucosal Injectable Solution by Micro-Tech (Nanjing) Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Injectable charcoal tattoo marker.

Cleared under the same submission

K200071 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Micro-Tech (Nanjing) Co., Ltd.

Sources (1)

  • FDA UDI 1e9480ba-4391-4406-8ec6-a9ebcdae4ca4 36 fields · synced Jun 6, 2026