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BGEcare

FDA UDI

Class II (US FDA UDI)

by Boston Bgecare Inc

Identity

Trade Name
BGEcare FDA UDI
Generic Name
Compression/pressure sock/stocking, reusable FDA UDI
Device Name
Anti-Embolism Stockings Knee High Open Toe X-Large FDA UDI
Description
Anti-Embolism Stockings Knee High Open Toe X-Large FDA UDI

Identifiers

Primary DI / UDI-DI
00850006820085 FDA UDI
FDA Product Code
DWL FDA UDI
GMDN Term
Compression/pressure sock/stocking, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5780 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Compression/pressure sock/stocking, reusable

BGEcare by Boston Bgecare Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Compression/pressure sock/stocking, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boston Bgecare Inc

Sources (1)

  • FDA UDI ac667735-c855-4771-9505-2d6b36dd3bd2 32 fields · synced Jun 8, 2026