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EasyPass

FDA UDI

Class I (US FDA UDI)

by Hangzhou Rejoin Mastin Medical Device Co., Ltd.

Identity

Trade Name
EasyPass FDA UDI
Generic Name
Suturing unit, single-use FDA UDI
Device Name
EasyPass Suture Passers, Frog, 45° Right 205mm FDA UDI
Model / Reference
810500100 FDA UDI
Description
EasyPass Suture Passers, Frog, 45° Right 205mm FDA UDI

Identifiers

Primary DI / UDI-DI
06973877665341 FDA UDI
FDA Product Code
HWQ FDA UDI
GMDN Term
Suturing unit, 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

Category: Suturing unit, single-use

EasyPass 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 Suturing unit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ead1f2c4-ca7f-46aa-870a-bba0ffd6ee28 33 fields · synced May 30, 2026