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Beauty Pack Evo

FDA UDI

Class II (US FDA UDI)

by Bemer Int. AG

Identity

Trade Name
Beauty Pack Evo FDA UDI
Generic Name
Light-energy skin surface treatment system applicator FDA UDI
Model / Reference
BEMER Therapy System Evo FDA UDI

Identifiers

Catalog Number
415020 FDA UDI
Primary DI / UDI-DI
07640161464124 FDA UDI
510(k) Number
K223919 FDA UDI
FDA Product Code
OHS FDA UDI
OLP FDA UDI
GMDN Term
Light-energy skin surface treatment system applicator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Light-energy skin surface treatment system applicator

Beauty Pack Evo by Bemer Int. AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Light-energy skin surface treatment system applicator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bemer Int. AG

Sources (1)

  • FDA UDI 2752b329-5077-4742-bfd4-a3fa8b9972a7 34 fields · synced Jun 8, 2026