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Compression Stocking

FDA UDI

Class II (US FDA UDI)

by Gottfried Medical, Inc.

Identity

Trade Name
Compression Stocking FDA UDI
Generic Name
Compression/pressure sock/stocking, reusable FDA UDI
Device Name
Arm Sleeve with Shoulder Flap FDA UDI
Model / Reference
103 FDA UDI
Description
Arm Sleeve with Shoulder Flap FDA UDI

Identifiers

Catalog Number
103 FDA UDI
Primary DI / UDI-DI
G420103 FDA UDI
510(k) Number
K823737 FDA UDI
FDA Product Code
DWL FDA UDI
FQL 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Compression/pressure sock/stocking, reusable

Compression Stocking by Gottfried Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 007cb78e-938d-4664-ae4d-ce8a0e053fda 35 fields · synced Jun 8, 2026