Identity
- Trade Name
- KS-Loading Forceps FDA UDI
- Generic Name
- Ophthalmic implant handling forceps, reusable FDA UDI
- Model / Reference
- 37-0088 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00883475954814 FDA UDI
- FDA Product Code
- HNR FDA UDI
- GMDN Term
- Ophthalmic implant handling forceps, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4350 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Ophthalmic implant handling forceps, reusable
KS-Loading Forceps by Charmant Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Ophthalmic implant handling forceps, reusable.
- Diamatrix — Diamatrix · Class I
- Stephens Instruments — KRISHNA IMPORTS INC · Class I
- VRTIS KAWAI PICK FORCEPS 23 GAUGE — Katena Products, Inc. · Class I
- Oph.Forceps — Katena Products, Inc. · Class I
- Ophthalmic Forceps — Katena Products, Inc. · Class I
- Ophthalmic Forceps — Katena Products, Inc. · Class I
- Stephens Instruments — KRISHNA IMPORTS INC · Class I
- Oph.Forceps — Katena Products, 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
- Charmant Inc.
Sources (1)
- FDA UDI 0e97391b-2eaf-4a69-8346-4a6eea94175a 32 fields · synced May 30, 2026