Identity
- Trade Name
- RapidLink FDA UDI
- Generic Name
- Suture knot pusher, single-use FDA UDI
- Device Name
- Kont pusher & suture cutter( 2-0#&0#) FDA UDI
- Model / Reference
- 810600200 FDA UDI
- Description
- Kont pusher & suture cutter( 2-0#&0#) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06970399633780 FDA UDI
- FDA Product Code
- HXO FDA UDI
- GMDN Term
- Suture knot pusher, 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: Suture knot pusher, single-use
RapidLink 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 Suture knot pusher, single-use.
- EKCOMED — Ekcomed Inc. · Class I
- FAST-FIX — Smith & Nephew, Inc. · Class I
- Lariat RS — ATRICURE, INC. · Class II
- Lariat RS — ATRICURE, INC. · Class I
- FAST-FIX — Smith & Nephew, Inc. · Class I
- Eclipse — Medshape, Inc. · Class I
- LaproShark — BRAINCHILD SURGICAL DEVICES LLC · Class I
- FAST-FIX — Smith & Nephew, Inc. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Hangzhou Rejoin Mastin Medical Device Co., Ltd.
Sources (1)
- FDA UDI 9217af61-f547-41d4-bd81-0d00b1f53ce9 33 fields · synced May 31, 2026