← Back to catalogue

RemoHip

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 801943300

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
Hip Tissue Elevator FDA UDI
Model / Reference
801943300 EUDAMEDFDA UDI
Description
Hip Tissue Elevator FDA UDI

Identifiers

Primary DI / UDI-DI
06973877662586 EUDAMED
06973877662739 FDA UDI
Basic UDI-DI
69418325P2021036159A EUDAMED
Direct Marketing DI
06973877662586 EUDAMED
FDA Product Code
HWL FDA UDI
EMDN Code
L1901 ARTHROSCOPIC SURGERY DISSECTORS, 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 ce0e1ed1-0d85-40c6-99bd-c4b36e701b91 33 fields · synced Oct 6, 2026
  • EUDAMED 08717a8f-4ae3-49b9-9b78-80ce4fdc6279 61 fields · synced Jul 28, 2026