CARDINAL HEALTH
- Primary DI
- 50888439920633
- Brand
- CARDINAL HEALTH
- Company
- Cardinal Health 200, LLC
- Model
- FGS-049
- Catalog number
- FGS-049
- Device description
- RETRACTOR MATHIEU BL 6.5IN ST
- Published
- 2021-07-09
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Product Codes#
| Code | Name |
|---|---|
| GAD | RETRACTOR |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| GAD | Retractor | General, Plastic Surgery | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 50888439920633 | Package | GS1 | 20 | In Commercial Distribution |
| 10888439920635 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 50888439920633 | 50888439920633 |
| 10888439920635 | 10888439920635 |
GMDN Terms#
| Term | Definition |
|---|---|
| Hand-held surgical retractor, single-use | A hand-held, non-self-retaining surgical instrument intended to be used to separate/draw aside the margins of a wound/incision to allow access to tissues/organs during open surgery; it is not dedicated to ophthalmic surgery or small nerve/vessel retraction, but may otherwise be clinically dedicated. It includes a shaped/hooked blade with a handle/holding portion and is available in a wide variety of designs, such as a double- or single-ended blade that may be fenestrated (pronged); deep wound retractors are typically designed with a long, curved blade that may also be intended to retract organs; it may include a light. This is a single-use device. |
Sterilization Methods#
| Method |
|---|
Regulatory Flags#
- DUNS number
- 961027315
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- true
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- true
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- true
- Sterilization required before use
- false
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 10192253047981 | Kendall | 9236 | 9236 | 2026-06-09 |
| 10192253047998 | Kendall | 9238 | 9238 | 2026-06-09 |
| 10192253048001 | Kendall | 9239 | 9239 | 2026-06-09 |
| 10192253048018 | Kendall | 9240 | 9240 | 2026-06-09 |
| 10192253048025 | Kendall | 9242 | 9242 | 2026-06-09 |
| 10192253048032 | Kendall | 9243 | 9243 | 2026-06-09 |
| 10192253046205 | Webcol | 5110 | 5110 | 2024-09-05 |
| 10192253047066 | Webcol | 6818 | 6818- | 2025-06-10 |
| 10192253047073 | Webcol | 6818-1 | 6818-1 | 2025-07-28 |
| 10884521008427 | Dover | 5027 | 5027 | 2016-09-24 |
| 10885380052538 | CARDINAL HEALTH | C-CB2S | C-CB2S | 2023-08-07 |
| 10885380052545 | CARDINAL HEALTH | C-CB3S | C-CB3S | 2023-08-07 |
| 10885380052569 | CARDINAL HEALTH | C-CB6S | C-CB6S | 2023-08-07 |
| 10885380052613 | CARDINAL HEALTH | C-CB6 | C-CB6 | 2023-08-07 |
| 10885380107801 | CARDINAL HEALTH | ABP1201 | ABP1201 | 2016-07-22 |
| 10885380107818 | CARDINAL HEALTH | ASC1201 | ASC1201 | 2016-07-22 |
| 10885380107825 | CARDINAL HEALTH | ASC1210 | ASC1210 | 2016-07-22 |
| 10885380107832 | CARDINAL HEALTH | ASC1211 | ASC1211 | 2016-07-22 |
| 10885380107849 | CARDINAL HEALTH | ASC1220 | ASC1220 | 2016-07-22 |
| 10885380107856 | CARDINAL HEALTH | ASC1221 | ASC1221 | 2016-07-22 |
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|---|---|---|---|---|
| 00198506091339 | ELMED INCORPORATED | ELMED INCORPORATED | GAD | 2026-06-09 |
| 00840277133670 | Innomed, Inc. | INNOMED, INC. | GAD | 2026-06-09 |
| 04049047155324 | Gimmi | Gimmi GmbH | GAD | 2026-06-08 |
| G453PM1580030BC0 | PEAK MEDICAL | Peak Medical Distribution Inc. | GAD | 2026-06-08 |
| 00846159040524 | SCANLAN® Retractor | SCANLAN INTERNATIONAL INC | GAD | 2026-06-04 |
| 00846159040531 | SCANLAN® Retractor | SCANLAN INTERNATIONAL INC | GAD | 2026-06-04 |
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