Identity
- Trade Name
- halo FDA UDI
- Generic Name
- X-ray system tube support, ceiling mounted FDA UDI
- Device Name
- tube mount, x-ray, diagnostic HQNR FDA UDI
- Model / Reference
- 02000 FDA UDI
- Description
- tube mount, x-ray, diagnostic HQNR FDA UDI
Identifiers
- Catalog Number
- 02000 FDA UDI
- Primary DI / UDI-DI
- 00863897000344 FDA UDI
- FDA Product Code
- IYB FDA UDI
- GMDN Term
- X-ray system tube support, ceiling mounted FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 892.1770 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
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Category: X-ray system tube support, ceiling mounted
halo by Core Labs, Llc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Del Medical/Universal — DEL MEDICAL, INC. · Class I
- Del Medical/Universal — DEL MEDICAL, INC. · Class I
- CH-200M — Shimadzu Corp. · 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 |
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Manufacturer
- Manufacturer
- Core Labs, Llc.
Sources (1)
- FDA UDI b88bc89e-c5af-4eb6-b284-17e20f10f56f 35 fields · synced May 31, 2026