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AccuBlade

FDA UDI

Class I (US FDA UDI)

by Hangzhou Rejoin Mastin Medical Device Co., Ltd.

Identity

Trade Name
AccuBlade FDA UDI
Generic Name
Arthroscopic shaver system blade, single-use FDA UDI
Device Name
AccuBlade 4.2mm Super Synovium, SN FDA UDI
Model / Reference
800200600 FDA UDI
Description
AccuBlade 4.2mm Super Synovium, SN FDA UDI

Identifiers

Primary DI / UDI-DI
06972884984704 FDA UDI
FDA Product Code
HTT FDA UDI
GMDN Term
Arthroscopic shaver system blade, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Arthroscopic shaver system blade, single-use

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

Similar devices

Also classified as Arthroscopic shaver system blade, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hangzhou Rejoin Mastin Medical Device Co., Ltd.

Sources (1)

  • FDA UDI db59612f-afe8-4bb1-8dcb-8a43a15e5504 33 fields · synced Jun 8, 2026