N/A
- Primary DI
- B089B61121XT0
- Brand
- N/A
- Company
- BLACK & BLACK SURGICAL, INC.
- Model
- B61121-XT
- Catalog number
- B61121-XT
- Device description
- LUMIVIEW "MIDI" RETRACTOR BLADE; 1 1/4"(30MM) X 5 3/8"(13.5CM), WITHOUT SERRATIONS
- Published
- 2022-09-12
- 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
- false
Product Codes
| Code | Name |
|---|
| FDG | RETRACTOR, FIBEROPTIC |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| FDG | Retractor, Fiberoptic | Gastroenterology, Urology | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| B089B61121XT0 | Primary | HIBCC | 0 | |
GMDN Terms
| Term | Definition |
|---|
| Surgical retractor/retraction system blade, reusable | A distal component of a surgical retraction system, surgical retractor, and/or surgical instrument assist arm system designed to function as a parting edge to separate the margins of a wound/incision during a surgical procedure. It is intended to be attached to the frame (e.g., mounting ring/bar) of a surgical retraction system, or may be fixed onto a retractor handle; it does not include a handle. It is a metal device, sometimes referred to as a variable or vario retractor blade when assembled with a separate retractor handle, because it is available in a variety of lengths and sizes. This is a reusable device. |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Regulatory Flags
- DUNS number
- 004382282
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- true
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