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Optomic

FDA UDI

Class I (US FDA UDI)

by Optomic España Sa

Identity

Trade Name
Optomic FDA UDI
Generic Name
General examination/treatment chair, electric FDA UDI
Model / Reference
OP-G7+N CHAIR (GOEPEL) FDA UDI

Identifiers

Primary DI / UDI-DI
08436041580683 FDA UDI
FDA Product Code
GBB FDA UDI
GMDN Term
General examination/treatment 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: General examination/treatment chair, electric

Optomic by Optomic España Sa — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General examination/treatment chair, electric.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Optomic España Sa

Sources (1)

  • FDA UDI 6f573d81-371b-4ea1-8fc1-5c87f5c888cc 32 fields · synced Jun 6, 2026