Identity
- Trade Name
- RONDO' FDA UDI
- Generic Name
- Bone holding forceps FDA UDI
- Model / Reference
- Bone holding forceps, self-centering FDA UDI
Identifiers
- Catalog Number
- VP-92203 FDA UDI
- Primary DI / UDI-DI
- 08056711928623 FDA UDI
- 510(k) Number
- K113388 FDA UDI
- FDA Product Code
- HWC FDA UDI
- GMDN Term
- Bone holding forceps FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3040 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
No
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: Bone holding forceps
Rondo' by Citieffe — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bone holding forceps.
- Millennium — AVALIGN TECHNOLOGIES, Inc. · Class I
- gSource — GSOURCE, LLC. · Class I
- Thrust Arm, Left, Pelvic Linear Hook Attachment — I.T.S. GmbH · Class I
- FORCEPS — KLS-Martin L.P. · Class I
- Integra® Jarit® — Integra LifeSciences Production Corporation · Class I
- CLAMP — KLS-Martin L.P. · Class I
- Novo Surgical — NOVO SURGICAL, INC. · Class I
- Tecomet — Tecomet,Inc · Class I
Cleared under the same submission
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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Citieffe
Sources (1)
- FDA UDI 92be4822-7533-48a8-931e-2c4c5d7fd68d 35 fields · synced May 31, 2026