Identity
- Trade Name
- KIATO PLUS FDA UDI
- Generic Name
- Manual scalpel blade, single-use FDA UDI
- Device Name
- KIATO PLUS Sterile Stainless Steel Surgical Blade box of 100 size 12d. Sterilized by Gamma Irradiation. FDA UDI
- Model / Reference
- 12d FDA UDI
- Description
- KIATO PLUS Sterile Stainless Steel Surgical Blade box of 100 size 12d. Sterilized by Gamma Irradiation. FDA UDI
Identifiers
- Catalog Number
- 18125KIATO PLUS Sterile Stainless Steel Surgical Blade box of 100 size 10. Steri FDA UDI
- Primary DI / UDI-DI
- 08902895181258 FDA UDI
- FDA Product Code
- GES FDA UDI
- GMDN Term
- Manual scalpel blade, 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
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
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Manual scalpel blade, single-use
The KIATO PLUS Sterile Stainless Steel Surgical Blade is a high-quality, single-use instrument designed for general surgery procedures. It features a sturdy stainless steel blade and a retractable protective guard for enhanced safety.
Similar devices
Also classified as Manual scalpel blade, single-use.
- Paramount — Paramount Surgimed Limited · Class IIa
- Bard-Parker ® Carbon Rib-Back Blades — Aspen Surgical Products, Inc. · Class I
- Swann-Morton — Swann-Morton Ltd · Class IIa
- SHARD — APPLIED DENTAL, INC. · Class I
- Sterile Stainless Blades — Southmedic Incorporated · Class I
- Paramount — Paramount Surgimed Limited · Class IIa
- Swann-Morton — Swann-Morton Ltd · Class IIa
- SHARD — APPLIED DENTAL, 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
- Aditya Dispomed Products Private Limited
Sources (1)
- FDA UDI 9c6b358b-2564-42fa-b00c-6472edd1062a 35 fields · synced Oct 6, 2026