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BRACOO KB30 Knee Fulcrum Wrap Dual Splints Stablizer w/Fixation Pad

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 0Model KE60

by Comfy Health Group Co., Ltd.

Identity

Trade Name
BRACOO KB30 Knee Fulcrum Wrap Dual Splints Stablizer w/Fixation Pad EUDAMED
ComfyHealth FDA UDI
Generic Name
Multiple-joint lower limb orthosis FDA UDI
Device Name
BRACOO KE60 Knee Airy Sleeve Breathable & Stabilizer w/ Ergo Cushion Pad Gary XL-Size EUDAMED
BRACOO KB30 Knee Fulcrum Wrap Dual Splints Stablizer w/Fixation Pad FDA UDI
Model / Reference
KE60 EUDAMED
0 EUDAMED
KB30 FDA UDI
Description
BRACOO KB30 Knee Fulcrum Wrap Dual Splints Stablizer w/Fixation Pad FDA UDI

Identifiers

Primary DI / UDI-DI
04719879642391 EUDAMEDFDA UDI
Basic UDI-DI
471987964KXXXVT EUDAMED
Direct Marketing DI
04719879642391 EUDAMED
FDA Product Code
IQI FDA UDI
ITQ FDA UDI
EMDN Code
M030499 ELASTIC BANDAGES, SUPPORT AND COMPRESSION - OTHER EUDAMED
GMDN Term
Multiple-joint lower limb orthosis FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
890.3475 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Compression/pressure sock/stocking, reusable

BRACOO KB30 Knee Fulcrum Wrap Dual Splints Stablizer w/Fixation Pad by Comfy Health Group Co., Ltd. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

Similar devices

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

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
TW-MF-000047382
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (2)

  • EUDAMED cdc3b858-823c-4255-8dce-b18d2ef8d6c1 61 fields · synced Jun 20, 2026
  • FDA UDI 998234eb-7d33-45d4-b0b7-18effe39a7b9 33 fields · synced May 30, 2026