Fisherbrand
- Primary DI
- 00613647010372
- Brand
- Fisherbrand
- Company
- FISHER SCIENTIFIC COMPANY L.L.C.
- Model
- 2850110TFC
- Catalog number
- 13812218
- Device description
- FISHERBRAND SPATULA R/T PTFE
- Published
- 2022-09-19
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- false
- OTC
- true
- Sterile
- false
- Single use
- false
Product Codes
| Code | Name |
|---|
| GAF | SPATULA, SURGICAL, GENERAL & PLASTIC SURGERY |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| GAF | Spatula, Surgical, General & Plastic Surgery | General, Plastic Surgery | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 00613647010372 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|
| 00613647010372 | 00613647010372 | 613647010372 | 0613647010372 |
GMDN Terms
| Term | Definition |
|---|
| General-purpose surgical spatula | A hand-held manual surgical instrument designed to manipulate tissue during various types of surgical interventions. It typically consists of a flat blunt blade (no sharp edges) that is double-ended (a blade at either end) and is not constructed for one particular part of the anatomy or clinical specialty. It is usually made of high-grade stainless steel and is available with a variety of blade designs, e.g., curved and flat or straight and flat with rounded ends; some blade types may be more right-angled. The handle will be formed from its middle section and may be more prominent/serrated. This is a reusable device. |
Regulatory Flags
- DUNS number
- 004321519
- Device count
- 1
- DM exempt
- true
- 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
- false
Other Devices From This Company
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|---|
| 00840018668164 | Nordent Manufacturing, Inc. | NORDENT MANUFACTURING INC | GAF | 2026-02-10 |
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| B382SD9150391050 | Surgical Direct | Surgical Direct, Inc. | GAF | 2025-12-29 |
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| B382SD915095250 | Surgical Direct | Surgical Direct, Inc. | GAF | 2025-12-29 |
| 00810158217263 | PRINCETON | Princeton Medical Group, Inc. | GAF | 2025-09-25 |
| 04250676741431 | Spatula | Spiggle & Theis Medizintechnik GmbH | GAF | 2025-09-24 |
| 04250676741448 | Spatula | Spiggle & Theis Medizintechnik GmbH | GAF | 2025-09-24 |
| 04250676741455 | Spatula | Spiggle & Theis Medizintechnik GmbH | GAF | 2025-09-24 |
| B382SD915095450 | Surgical Direct | Surgical Direct, Inc. | GAF | 2025-08-11 |
| 00840343725792 | GEN2 | SURGIX MEDICAL LLC | GAF | 2025-06-16 |
| 00840343725808 | GEN2 | SURGIX MEDICAL LLC | GAF | 2025-06-16 |
| 00840343725815 | GEN2 | SURGIX MEDICAL LLC | GAF | 2025-06-16 |
| 50649111448612 | Sklar Instruments | SKLAR CORPORATION | GAF | 2025-05-29 |
| B382SD915039100 | Surgical Direct | Surgical Direct, Inc. | GAF | 2025-05-19 |
| B382SD915039120 | Surgical Direct | Surgical Direct, Inc. | GAF | 2025-05-19 |
| B382SD9150471110 | Surgical Direct | Surgical Direct, Inc. | GAF | 2025-05-19 |
| 04049047034964 | Gimmi | Gimmi GmbH | GAF | 2025-05-06 |
| B382SD1552400 | Surgical Direct | Surgical Direct, Inc. | GAF | 2025-05-05 |
| B382SD1552420 | Surgical Direct | Surgical Direct, Inc. | GAF | 2025-05-05 |
| B382SD1552440 | Surgical Direct | Surgical Direct, Inc. | GAF | 2025-05-05 |
| B356KF411240 | American Medicals | American Medicals | GAF | 2025-04-18 |
| 00840343725761 | GEN2 | SURGIX MEDICAL LLC | GAF | 2025-02-25 |
| 00840343725778 | GEN2 | SURGIX MEDICAL LLC | GAF | 2025-02-25 |
| 00840343725785 | GEN2 | SURGIX MEDICAL LLC | GAF | 2025-02-25 |
| 00810158214101 | PRINCETON | Princeton Medical Group, Inc. | GAF | 2025-01-21 |