Identity
- Trade Name
- DeRoyal FDA UDI
- Generic Name
- Laparoscopic blunt dissector FDA UDI
- Device Name
- Custom Kaiser Snares FDA UDI
- Model / Reference
- 32-1266 FDA UDI
- Description
- Custom Kaiser Snares FDA UDI
Identifiers
- Catalog Number
- 32-1266 FDA UDI
- Primary DI / UDI-DI
- 00749756042147 FDA UDI
- FDA Product Code
- GAE FDA UDI
- GMDN Term
- Laparoscopic blunt dissector 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
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Laparoscopic blunt dissector
DeRoyal by Deroyal Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Laparoscopic blunt dissector.
- Snowden-Pencer — STERIS CORPORATION · Class II
- Flex — Medrobotics Corporation · Class II
- Medline — MEDLINE INDUSTRIES, INC. · Class II
- MEDLINE — MEDLINE INDUSTRIES, INC. · U
- CORE DYNAMICS — Conmed Corporation · Class II
- FLEX — Medrobotics Corporation · Class II
- CORE DYNAMICS — Conmed Corporation · Class II
- Snowden-Pencer — STERIS CORPORATION · Class II
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
- Deroyal Industries, Inc.
Sources (1)
- FDA UDI cb0f2912-8327-4a9d-bcf3-defc1f58615b 35 fields · synced Jun 8, 2026