← Back to catalogue

Baylis Medical Company Radiofrequency Puncture Generator

FDA UDIEUDAMED

Class II (US FDA UDI)

by Baylis Médicale Cie Inc

Identity

Trade Name
Baylis Medical Company Radiofrequency Puncture Generator FDA UDI
Generic Name
Electrosurgical system generator FDA UDI
Model / Reference
RFP-100A FDA UDI

Identifiers

Primary DI / UDI-DI
00685447000969 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrosurgical system generator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrosurgical system generator

Baylis Medical Company Radiofrequency Puncture Generator by Baylis Médicale Cie Inc — Class II — MDD, FDA UDI — listed in FDA GUDID, EUDAMED

Similar devices

Also classified as Electrosurgical system generator.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (2)

  • FDA UDI 9f6a6dbb-f64f-4c6c-9d58-3a5ec5563279 32 fields · synced Jun 19, 2026
  • EUDAMED 1 fields · synced Jun 19, 2026