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SST Pro

FDA UDI

Class I (US FDA UDI)

by SeoulinMedicare Co., Ltd.

Identity

Trade Name
SST Pro FDA UDI
Generic Name
Hair extraction punch FDA UDI
Model / Reference
SLM-1001 FDA UDI

Identifiers

Primary DI / UDI-DI
08800066110017 FDA UDI
FDA Product Code
GEY FDA UDI
GMDN Term
Hair extraction punch FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Hair extraction punch

SST Pro by SeoulinMedicare Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hair extraction punch.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1ec7fa1a-be5f-4388-8f4a-444f0621fa17 32 fields · synced May 30, 2026