← Back to catalogue

amazon basic care

FDA UDI

Class II (US FDA UDI)

by Amazon.com Services, LLC

Identity

Trade Name
amazon basic care FDA UDI
Generic Name
Compression/pressure sock/stocking, single-use FDA UDI
Device Name
Medical Compression Stockings, 20-30 mmHg Support, Women & Men Thigh Length Hose, Open Toe, Beige, 2X-Large FDA UDI
Model / Reference
AB_0868BG-2L FDA UDI
Description
Medical Compression Stockings, 20-30 mmHg Support, Women & Men Thigh Length Hose, Open Toe, Beige, 2X-Large FDA UDI

Identifiers

Primary DI / UDI-DI
00195515025836 FDA UDI
FDA Product Code
DWL FDA UDI
GMDN Term
Compression/pressure sock/stocking, single-use 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

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Compression/pressure sock/stocking, single-use

amazon basic care by Amazon.com Services, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Compression/pressure sock/stocking, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 128c582f-cd96-4559-ae85-6e7a38a6527e 33 fields · synced May 30, 2026