| Primary Device ID | 04260029580259 |
| NIH Device Record Key | 9bb7ef87-6705-43a0-8f4f-080a4bad7782 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Pectus Bar Template, 229 mm |
| Version Model Number | 021-09229 |
| Catalog Number | 021-09229 |
| Company DUNS | 331019344 |
| Company Name | MedXpert GmbH |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +4976345085630 |
| ask-the-xpert@medXpert.de |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04260029580259 [Primary] |
| MDM | Instrument, Manual, Surgical, General Use |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[04260029580259]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-06-26 |
| Device Publish Date | 2017-01-09 |
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| 04260029586572 - Pectus Bar Stabilizer, Universal, L, 2 x Ø4x8 mm | 2018-08-10 |
| 04260029580204 - Pectus Allergy Test Plate | 2018-06-26 |
| 04260029580235 - Pectus Bar Template, 178 mm | 2018-06-26 |
| 04260029580242 - Pectus Bar Template, 203 mm | 2018-06-26 |
| 04260029580259 - Pectus Bar Template, 229 mm | 2018-06-26 |
| 04260029580259 - Pectus Bar Template, 229 mm | 2018-06-26 |