CONTIPLEX®
- Primary DI
- 04046964176982
- Brand
- CONTIPLEX®
- Company
- B. BRAUN MEDICAL INC.
- Model
- 331706
- Catalog number
- 331706
- Device description
- Contiplex® Tuohy Tray (Kit), 18 Ga. x 4 in. Insulated Needle and Non-Stimulating Catheter (CNB400TK)
- Published
- 2016-09-23
- Public version status
- Update
- Distribution status
- Not in Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| CAZ | Anesthesia conduction kit |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| CAZ | Anesthesia Conduction Kit | Anesthesiology | 2 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 04046964176982 | Primary | GS1 | 0 | |
| 04046964176975 | Unit of Use | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 04046964176982 | 04046964176982 | 4046964176982 |
| 04046964176975 | 04046964176975 | 4046964176975 |
GMDN Terms#
| Term | Definition |
|---|---|
| Peripheral anaesthesia catheter set, non-medicated | A collection of devices intended for the continuous-administration of an anaesthetic agent (not included) to function as a peripheral nerve-block. It includes an anaesthesia needle and an anaesthesia catheter usually with additional devices utilized for the procedure (e.g., connectors, catheter holder). This is a single-use device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 | |
| Device Size Text, specify | 0 |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Handling Environment Temperature | 0 | 0 | |
| Storage Environment Temperature | 0 | 0 |
Contacts#
| Phone | |
|---|---|
| +1(800)227-2862 | BBMUS_Service.EmailOrders@bbraun.com |
Regulatory Flags#
- DUNS number
- 002397347
- Device count
- 10
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- true
- Combination product
- true
- 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
- true
- Sterilization required before use
- false
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 04022495101211 | Stimuplex® | 4894260 | 4894260 | 2016-09-23 |
| 04046955966295 | Design Options® | 552210 | 552210 | 2026-10-18 |
| 04022495101167 | Stimuplex® | 4894251 | 4894251 | 2016-09-23 |
| 04022495101266 | Stimuplex® | 4894278 | 4894278 | 2016-09-23 |
| 04022495101310 | Stimuplex® | 4894502 | 4894502 | 2016-09-23 |
| 04022495166579 | Stimuplex® | 4894367 | 4894367 | 2016-09-23 |
| 04022495187826 | Stimuplex® | 4894539 | 4894539 | 2016-09-23 |
| 04046955665075 | Extension Set | 490630 | 490630 | 2021-02-08 |
| 04046964991257 | Extension Set | 490486 | 490486 | 2017-04-03 |
| 04046955270347 | IV Administration Set | 490550 | 490550 | 2019-02-22 |
| 04046955287475 | IV Administration Set | 490574 | 490574 | 2018-10-05 |
| 04046955203307 | IV Administration Set | 490529 | 490529 | 2018-06-15 |
| 04046964296734 | Extension Set | 456522 | 456522 | 2016-09-23 |
| 04046955874330 | INTROCAN SAFETY® | 4251610-02 | 4251610-02 | 2026-10-11 |
| 04046955765164 | IV Administration Set | 490640 | 490640 | 2026-09-27 |
| 04046955114559 | IV Administration Set | 490501 | 490501 | 2026-09-19 |
| 04046955862658 | Design Options® | 552204 | 552204 | 2026-08-17 |
| 04046955966233 | Design Options® | 530209 | 530209 | 2026-08-17 |
| 04046955966370 | Design Options® | 570361 | 570361 | 2026-08-17 |
| 04046961025153 | Prontosan® | 400604 | 400604 | 2026-08-09 |
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| 10801902228083 | ARROW | TELEFLEX INCORPORATED | CAZ | 2026-10-09 |
| 10801902228090 | ARROW | TELEFLEX INCORPORATED | CAZ | 2026-10-09 |
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