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Sensory Cuff

FDA UDI

Class I (US FDA UDI)

by Therafin Corporation

Identity

Trade Name
Sensory Cuff FDA UDI
Generic Name
Compression/pressure shirt/pants FDA UDI
Device Name
CUFF, SENSORY SMALL PAIR (4"W X 10" L) FDA UDI
Model / Reference
30221 FDA UDI
Description
CUFF, SENSORY SMALL PAIR (4"W X 10" L) FDA UDI

Identifiers

Catalog Number
30221 FDA UDI
Primary DI / UDI-DI
00840252904042 FDA UDI
FDA Product Code
KNM FDA UDI
GMDN Term
Compression/pressure shirt/pants FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5765 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

Yes

FDA UDI

Category: Compression/pressure shirt/pants

Sensory Cuff by Therafin Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Compression/pressure shirt/pants.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e61fe1d5-7a99-4d3c-8e4e-b2b0dec8fcc3 35 fields · synced Jun 8, 2026