Identity
- Trade Name
- A. Titan Instruments FDA UDI
- Generic Name
- Nylon suture, non-bioabsorbable, monofilament FDA UDI
- Device Name
- Nylon, Monofilament, Non-Absorbable Suture, C-31 Needle, 18", 4-0 FDA UDI
- Model / Reference
- ATI-31-18-4MM FDA UDI
- Description
- Nylon, Monofilament, Non-Absorbable Suture, C-31 Needle, 18", 4-0 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00841685100339 FDA UDI
- FDA Product Code
- KDD FDA UDI
- GMDN Term
- Nylon suture, non-bioabsorbable, monofilament 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
No
FDA UDI
Single Use
No
FDA UDI
Implantable
Yes
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
Dry Heat Sterilization FDA UDI
Category: Nylon suture, non-bioabsorbable, monofilament
A. Titan Instruments by A.Titan Instruments — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 |
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Manufacturer
- Manufacturer
- A.Titan Instruments
Sources (1)
- FDA UDI 9bb025af-f5ce-4fb9-b403-63bf071508eb 33 fields · synced Jun 9, 2026