Identity
- Trade Name
- PILLING FDA UDI
- Generic Name
- Suturing needle, reusable FDA UDI
- Device Name
- NEEDLE RHOTON STR 7.5" FDA UDI
- Model / Reference
- IPN019354 FDA UDI
- Description
- NEEDLE RHOTON STR 7.5" FDA UDI
Identifiers
- Catalog Number
- P21362 FDA UDI
- Primary DI / UDI-DI
- 14026704796929 FDA UDI
- FDA Product Code
- HAS FDA UDI
- GMDN Term
- Suturing needle, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 882.4650 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
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Suturing needle, reusable
Pilling by Teleflex Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Suturing needle, reusable.
- STOMA® — Storz am Mark GmbH · Class I
- Novo Surgical — NOVO SURGICAL, INC. · Class I
- MSI Precision Specialty Instruments — Med Saver, Inc. · Class I
- Hermann Medizintechnik GmbH — Hermann Medizintechnik GmbH · Class I
- Millennium — AVALIGN TECHNOLOGIES, Inc. · Class I
- Hayden Medical — Hayden Medical Inc · Class I
- FENTEX — FENTEX medical GmbH · Class I
- Hurd tonsil suture needle, right, 22 cm — Spiggle & Theis Medizintechnik GmbH · 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
- Teleflex Incorporated
Sources (1)
- FDA UDI 09e129c6-4b61-4e9a-a671-dc0008b938ee 35 fields · synced May 30, 2026