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CERAGEM Master V7

FDA UDI

Class II (US FDA UDI)

by Ceragem Co., Ltd.

Identity

Trade Name
CERAGEM Master V7 FDA UDI
Generic Name
Massage table/couch, line-powered FDA UDI
Model / Reference
CGM MB-2302 FDA UDI

Identifiers

Primary DI / UDI-DI
08809494000983 FDA UDI
510(k) Number
K243644 FDA UDI
FDA Product Code
JFB FDA UDI
IRP FDA UDI
GMDN Term
Massage table/couch, line-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5880 FDA UDI
890.5650 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Compression/pressure sock/stocking, reusableSequential venous compression system inflatorMassage table/couch, line-powered

CERAGEM Master V7 by Ceragem Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Massage table/couch, line-powered.

Cleared under the same submission

K243644 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ceragem Co., Ltd.

Sources (1)

  • FDA UDI 41a2b187-e3d1-45a6-871a-f91522fdaa57 33 fields · synced May 31, 2026