Identity
- Trade Name
- GRIP, STERILE FDA UDI
- Generic Name
- Suturing needle holder, single-use FDA UDI
- Device Name
- PUSH PIN FDA UDI
- Model / Reference
- 25-408-01-75 FDA UDI
- Description
- PUSH PIN FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10888118039993 FDA UDI
- FDA Product Code
- MDM FDA UDI
- GMDN Term
- Suturing needle holder, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
Yes
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
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Suturing needle holder, single-use
Grip, Sterile by KLS-Martin L.P. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Suturing needle holder, single-use.
- Devon — Cardinal Health 200, LLC · Class I
- Sklar Instruments — Sklar Corporation · Class I
- Needle Holder Troutman — BLINK MEDICAL LIMITED · Class I
- Sklar Instruments — Sklar Corporation · Class I
- Instrapac — ROBINSON HEALTHCARE LIMITED · Class I
- CROWN SURGICAL — CROWN SURGICAL CORPORATION · Class I
- Trinity Sterile, Inc. — TRINITY STERILE, INC. · Class I
- STRoPP — CROSSROADS EXTREMITY SYSTEMS LLC · Class II
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
- KLS-Martin L.P.
Sources (1)
- FDA UDI dd4c9303-b2e3-45cb-a4cd-7fc5acca081f 34 fields · synced Jun 6, 2026