| Primary Device ID | 05056785301455 |
| NIH Device Record Key | d448c528-3988-4078-9891-c994e03023f7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Paediatric Speculum Angled Temporal |
| Version Model Number | 31-3102 |
| Company DUNS | 738288096 |
| Company Name | BLINK MEDICAL LIMITED |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05056785301448 [Primary] |
| GS1 | 05056785301455 [Package] Contains: 05056785301448 Package: [10 Units] In Commercial Distribution |
| HNC | Specula, Ophthalmic |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-01-15 |
| Device Publish Date | 2025-01-07 |
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| 05056785301455 - Paediatric Speculum Angled Temporal | 2025-01-15 |
| 05056785301455 - Paediatric Speculum Angled Temporal | 2025-01-15 |
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| 05056785301363 - Den VA Cataract Instrument Pack | 2024-12-26 |
| 05060745559572 - Meibomian Gland Expression Forceps | 2024-10-16 |
| 05060745558940 - Scissors Suture Removal | 2024-06-20 |
| 05060480400009 - Forceps Angled Jewellers 4mm Tip | 2024-05-29 |
| 05060480400139 - Forceps Epilation Angled | 2024-05-29 |