By Category
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Catheters (6,800+)
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Infection Control (2,500+)
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- IV Therapy (2,000+)
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Medical Apparel (23,000+)
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PPE (20,000+)
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- Bleach (360+)
- Coveralls (500+)
- Disinfectant Wipes (350+)
- Face Shields (200+)
- Gloves (8,000+)
- Gowns (2,300+)
- Isopropyl Alcohol (170+)
- IV Therapy (2,000+)
- Masks (3,700+)
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- Sanitizer (670+)
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Wound Care (5,000+)
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By Brand
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- Medline (54,000+)
- Midmark (2,500+)
- Roche (300+)
- Smiths Medical (4,000+)
- Sunset Healthcare (450+)
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- View All Brands (5,000+)
Part Number
Fenwal 4R2014
SKU Number
CIA2261050
Sell Unit
CASE
Ships Within
Special Order
List Price
$1,582.10
Product Description
Fenwal 4R2014 - PACK, TRANSFER PACK UNITS 300ML, 96/CS
Transfer-Pack container with Coupler - 300 mL
For processing and/or storage of blood or blood components. Transfer-Pack containers in multiple configurations to address your needs. Dispensing cartons available on most Transfer-Packs.
- Sterile, nonpyrogenic fluid path.
- Sterilized by irradiation. Sterile fluid path.
- Do not use if tip protector is not in place.
- Dispose of container appropriately
- Single use only.
Instructions for Fluid Transfer: Use Aseptic Technique
- Prepare unit for desired fluid transfer, placing in plasma extractor if necessary.
- Clamp a hemostat on the Transfer Pack Container tubing.
- Expose outlet port of unit containing fluid.
- Remove coupler into outlet port with a twisting motion until firmly seated.
- Remove hemostat to initiate fluid transfer, if plasma extractor is used, release handle and gently allow plate to contact unit.
- When desired amount of fluid has been transferred, clamp hemostat on Transfer Pack Container tubing.
- Remove unit from plasma extractor if used. Make three hermetic seals closely spaced, on Transfer Pack Container tubing. Carefully sever center seal using care to avoid fluid splatter. Remove hemostat.
- Label containers appropriately and store as required.
Device Characteristics
| What MRI safety information does the labeling contain? | Labeling does not contain MRI Safety Information |
| Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437) | No |
| Device labeled as "Not made with natural rubber latex" | No |
| For Single-Use | Yes |
| Prescription Use (Rx) | Yes |
| Over the Counter (OTC) | No |
| Kit | No |
| Combination Product | No |
| Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P) | No |
