← Back to catalogue

RemoHip

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 801943500

by Hangzhou Rejoin Mastin Medical Device Co., Ltd.

Identity

Trade Name
RemoHip FDA UDI
Generic Name
Arthroscopic surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
Reusable Surgical Instruments EUDAMED
Rasp, 220mm FDA UDI
Model / Reference
801943500 EUDAMEDFDA UDI
Description
Rasp, 220mm FDA UDI

Identifiers

Primary DI / UDI-DI
06973877662593 EUDAMED
06973877662746 FDA UDI
Basic UDI-DI
69418325P2021036089D EUDAMED
Direct Marketing DI
06973877662593 EUDAMED
FDA Product Code
HWL FDA UDI
EMDN Code
L091201 ORTHOPAEDIC SURGERY RASPS, REUSABLE EUDAMED
GMDN Term
Arthroscopic surgical procedure kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.4540 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

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Arthroscopic surgical procedure kit, non-medicated, reusable

RemoHip by Hangzhou Rejoin Mastin Medical Device Co., Ltd. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Arthroscopic surgical procedure kit, non-medicated, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (2)

  • FDA UDI 2d99561e-63ca-4028-b405-b11dc464047d 33 fields · synced Jun 19, 2026
  • EUDAMED b52e1e35-f37c-40ca-a943-91725b834ba5 61 fields · synced Jun 19, 2026