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Vitalcontrol

FDA UDI

Class II (US FDA UDI)

by Beurer North America, L.p.

Identity

Trade Name
Vitalcontrol FDA UDI
Generic Name
Electric pad localized-body heating system FDA UDI
Device Name
IAN 366497_2101 Shoulder Heating Pad (Red) SHK 50 Art. No. 211.67/ EAN 4211125211677 Art. No. 277.80/ EAN 4211125277826 FDA UDI
Model / Reference
SHK50 (Red) FDA UDI
Description
IAN 366497_2101 Shoulder Heating Pad (Red) SHK 50 Art. No. 211.67/ EAN 4211125211677 Art. No. 277.80/ EAN 4211125277826 FDA UDI

Identifiers

Primary DI / UDI-DI
00850031772076 FDA UDI
FDA Product Code
IRT FDA UDI
GMDN Term
Electric pad localized-body heating system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5740 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

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: Electric pad localized-body heating system

Vitalcontrol by Beurer North America, L.p. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electric pad localized-body heating system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d709acb9-c2a7-496c-b8e1-097d53c0279b 34 fields · synced May 30, 2026