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Meet Blossom

FDA UDI

Class II (US FDA UDI)

by Sword Health, S.a.

Identity

Trade Name
Meet Blossom FDA UDI
Generic Name
Pelvic floor muscle exerciser FDA UDI
Model / Reference
1 FDA UDI

Identifiers

Primary DI / UDI-DI
05065013876047 FDA UDI
FDA Product Code
KXQ FDA UDI
GMDN Term
Pelvic floor muscle exerciser FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.5960 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

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: Pelvic floor muscle exerciser

Meet Blossom by Sword Health, S.a. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pelvic floor muscle exerciser.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sword Health, S.a.

Sources (1)

  • FDA UDI 7f83f9a4-83d3-45f1-9a37-937fd4353498 32 fields · synced Jun 8, 2026