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Venomed

FDA UDI

Class I (US FDA UDI)

by Pantymed S.a.

Identity

Trade Name
VENOMED FDA UDI
Generic Name
Compression/pressure sock/stocking, reusable FDA UDI
Device Name
MEDIA TERAPEUTICA HASTA LA ROD U XL FDA UDI
Model / Reference
1501-20RP U XL FDA UDI
Description
MEDIA TERAPEUTICA HASTA LA ROD U XL FDA UDI

Identifiers

Primary DI / UDI-DI
07798094548159 FDA UDI
FDA Product Code
FQL FDA UDI
GMDN Term
Compression/pressure sock/stocking, reusable FDA UDI

Classification

Device Class
Class I 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

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Compression/pressure sock/stocking, reusable

Venomed by Pantymed S.a. — Class I — 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
Pantymed S.a.

Sources (1)

  • FDA UDI d111ec6a-3ff4-40e2-9f2e-c543ca6be54f 33 fields · synced May 31, 2026