Instaform
- Primary DI
- 00628341931915
- Brand
- Instaform
- Company
- CDR Systems Inc
- Model
- 1
- Catalog number
- IF-01
- Device description
- INSTAFORM Water-Activated Custom Support Cushion - Size 01
- Published
- 2026-08-17
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| IYE | Accelerator, Linear, Medical |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| IYE | Accelerator, Linear, Medical | Radiology | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K122888 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10628341931912 | Package | GS1 | 25 | In Commercial Distribution |
| 00628341931915 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 10628341931912 | 10628341931912 | ||
| 00628341931915 | 00628341931915 | 628341931915 | 0628341931915 |
GMDN Terms#
| Term | Definition |
|---|---|
| Patient positioning foam mould kit | A collection of devices designed to facilitate the delivery of a self-hardening foam that is either poured or injected into a bag or container placed around a patient. After hardening, the foam and the bag/container form a patient-specific (custom-made) mould of that anatomy. The mould can be whole body or only selected body parts and are commonly used to help ensure adequate positioning and immobilization of the patient during radiation therapy treatments and to facilitate reproducible positioning for serial treatments. |
Contacts#
| Phone | |
|---|---|
| 403-850-7035 | info@cdrsys.ca |
Regulatory Flags#
- DUNS number
- 206950904
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00628341930512 | Extremity Lock | 1 | EXT-24STD | 2024-12-11 |
| 00628341930529 | Extremity Lock | 1 | EXT-24STD-K | 2025-01-21 |
| 00628341930352 | Freedom | 1 | PLUS | 2019-12-31 |
| 00628341930369 | Freedom | 1 | PLUS-K | 2019-12-31 |
| 00628341930413 | Solid Bolus | 1 | S-Bolus | 2025-01-21 |
| 10628341930410 | Solid Bolus | 1 | S-Bolus | 2025-01-21 |
| 10628341930526 | Extremity Lock | 1 | EB-24STD-K | 2025-01-21 |
| 10628341930519 | Extremity Lock | 1 | EB-24STD | 2024-12-11 |
| 00628341930505 | EQUILIBRIUM | 1 | 2024-01-25 | |
| 10628341930502 | EQUILIBRIUM | 1 | 2024-01-25 | |
| 00628341930376 | Thermoplastic | 1 | 2023-12-31 | |
| 00628341930383 | Thermoplastic | 1 | 2023-12-31 | |
| 10628341930373 | Thermoplastic | 1 | 2023-12-31 | |
| 10628341930380 | Thermoplastic | 1 | 2023-12-31 | |
| 00628341930482 | Freedom | 1 | AP2 | 2023-08-08 |
| 00628341930499 | Freedom | 1 | AP2-K | 2023-08-08 |
| 00628341930468 | TBI | 1 | TBI20 | 2023-03-08 |
| 10628341930465 | TBI | 1 | TBI20 | 2023-03-08 |
| 00628341930444 | Freedom | 1 | LBST | 2023-02-23 |
| 00628341930451 | Freedom | 1 | LBST-K | 2023-02-23 |
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| 00850065937205 | eMotus | EMPNIA INC. | IYE | 2026-09-21 |
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| 00850065937250 | eMotus | EMPNIA INC. | IYE | 2026-09-21 |
| 00850065937267 | eMotus | EMPNIA INC. | IYE | 2026-09-21 |
| 00850065937274 | eMotus | EMPNIA INC. | IYE | 2026-09-21 |
| 00850065937298 | eMotus | EMPNIA INC. | IYE | 2026-09-21 |
| 00850065937304 | eMotus | EMPNIA INC. | IYE | 2026-09-21 |