Identity
- Trade Name
- Optomic FDA UDI
- Generic Name
- ENT chair, electric FDA UDI
- Model / Reference
- OP-S9 CHAIR FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08436041581451 FDA UDI
- FDA Product Code
- GBB FDA UDI
- GMDN Term
- ENT chair, electric FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4960 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
No
FDA UDI
Category: ENT chair, electric
Optomic by Optomic España Sa — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as ENT chair, electric.
- JEDMED — JEDMED Instrument Company · Class I
- BR Surgical, LLC — BR SURGICAL LLC · Class I
- BR Surgical, LLC — BR SURGICAL LLC · Class I
- OTOPRONT — Happersberger Otopront GmbH · Class I
- BR Surgical, LLC — BR SURGICAL LLC · Class I
- BR Surgical, LLC — BR SURGICAL LLC · Class I
- BR Surgical, LLC — BR SURGICAL LLC · Class I
- BR Surgical, LLC — BR SURGICAL LLC · 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
- Optomic España Sa
Sources (1)
- FDA UDI aaae2617-468a-43d2-8101-78e269e0a0f1 32 fields · synced May 30, 2026