Identity
- Trade Name
- SU-VEID FDA UDI
- Generic Name
- Rib/rib cage internal fixation/bracing system bracing bar FDA UDI
- Device Name
- Carton of 16 boxes (DI# 07290018896136) of 30 SU-VEID units each (DI# 07290018896037) - for a total of 480 SU-VEID units per carton. FDA UDI
- Model / Reference
- 18103300 FDA UDI
- Description
- Carton of 16 boxes (DI# 07290018896136) of 30 SU-VEID units each (DI# 07290018896037) - for a total of 480 SU-VEID units per carton. FDA UDI
Identifiers
- Catalog Number
- 18103300 FDA UDI
- Primary DI / UDI-DI
- 07290018896235 FDA UDI
- 510(k) Number
- K993995 FDA UDI
- FDA Product Code
- FRF FDA UDI
- GMDN Term
- Rib/rib cage internal fixation/bracing system bracing bar FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5045 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Ethylene Oxide FDA UDI
Category: Rib/rib cage internal fixation/bracing system bracing bar
Su-Veid by Angie Technologies Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Rib/rib cage internal fixation/bracing system bracing bar.
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Cleared under the same submission
K993995 also covers:
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 |
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Manufacturer
- Manufacturer
- Angie Technologies Ltd
Sources (1)
- FDA UDI e20b58a5-8018-4a50-8c7a-b087ee68ad92 35 fields · synced May 30, 2026