32A

Radiofrequency identification transmitters

920–926

4 W

1. A transmitter mentioned in this item must comply with ISO/IEC 18000‑6c (RFID Gen. 2).

2. Emissions in the band below 917.75 MHz must be no greater than ‑37 dBm EIRP.

3. Emissions above 926 MHz must be no greater than ‑33 dBm EIRP.

4. A transmitter mentioned in this item must not be used unless more than 1 Watt EIRP is necessary to achieve satisfactory system performance.

Note   ISO/IEC 18000‑6c (RFID Gen. 2) refers to an international standard published by the International Organization for Standardization (ISO). The international standard is included in a document titled Information Technology — Radio frequency identification for item management — Part 6: Parameters for air interface communications at 860 MHz to 960 MHz. The document is numbered ISO/IEC 18000‑6:2004 and is available on the internet at http://www.saiglobal.com.

49

Medical implant communications systems transmitters

402–405

25 µW

1. The maximum EIRP applies outside the body.

2. A transmitter mentioned in this item must comply with ETSI EN 301 839‑2.

Note 1   The systems and associated medical implant communications systems transmitters mentioned in item 49 are devices that require marketing approval from the Therapeutic Goods Administration.

Note 2   At the time this item commenced,  ETSI EN 301 839‑2 referred to a standard titled Electromagnetic compatibility and Radio spectrum Matters (ERM); Short Range Devices (SRD); Ultra Low Power Active Medical Implants (ULP‑AMI) and Peripherals (ULP‑AMI‑P) operating in the frequency range 402 MHz to 405 MHz; Part 2 Harmonized EN covering essential requirements of article 3.2 of the R&TTE Directive. The standard is available on the internet at http://www.etsi.org.

49A

Medical implant communications systems transmitters

1. 401–402

2. 405–406

25 µW

1. The maximum EIRP applies outside the body.

2. A transmitter mentioned in this item must comply with ETSI EN 302 537‑2.

Note 1   The systems and associated medical implant communications systems transmitters mentioned in item 49A are devices that require marketing approval from the Therapeutic Goods Administration.

Note 2   At the time this item commenced, ETSI EN 302 537‑2 referred to a standard titled Electromagnetic compatibility and Radio spectrum Matters (ERM); Short Range Devices (SRD); Ultra Low Power Medical Data Service Systems operating in the frequency range 401 MHz to 402 MHz and 405 MHz to 406 MHz; Part 2: Harmonized EN covering essential requirements of article 3.2 of the R&TTE Directive. The standard is available on the internet at http://www.etsi.org.

58

Video sender transmitters

529–806

12 µW