UniMSK
- Primary DI
- 14048223036706
- Brand
- UniMSK
- Company
- Pajunk GmbH Medizintechnologie
- Model
- 1192-4E070
- Catalog number
- 1192-4E070
- Device description
- UniMSK 22G x 70mm with bevel tip and depth graduation,
- Published
- 2020-02-05
- 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
Related Records
Contact Domains
Product Codes
| Code | Name |
|---|---|
| BSP | NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| BSP | Needle, Conduction, Anesthetic (W/Wo Introducer) | Anesthesiology | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 14048223036706 | Primary | GS1 | 0 | |
| 04048223036709 | Unit of Use | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 14048223036706 | 14048223036706 | |
| 04048223036709 | 04048223036709 | 4048223036709 |
GMDN Terms
| Term | Definition |
|---|---|
| Peripheral nerve-block sharp needle | A sterile, sharp bevel-edged, hollow tubular metal instrument intended to invasively access a peripheral nerve to inject an anaesthetic/analgesic agent for nerve-block/pain control (e.g., sleeve blocks, deep muscle blocks, hypogastric blocks, paravertebral blocks, joint blocks, selective nerve root, lumbar sympathetic, Coeliac plexus). It may be used to deliver anaesthetic or analgesic agents directly and/or to allow introduction of a dedicated catheter for administration. This is a single-use device. |
Sterilization Methods
| Method |
|---|
Contacts
| Phone | |
|---|---|
| +1(888)972-5865 | info@pajunk-usa.com |
Regulatory Flags
- DUNS number
- 317654283
- Device count
- 10
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- 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
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|---|---|---|---|---|
| 04048223126103 | NerveStim Pure | 1151-94-90 | 1151-94-90 | 2026-02-06 |
| 04048223128817 | SPROTTE® | 511151-29A | 511151-29A | 2025-09-16 |
| 04048223129111 | SPROTTE® NRFit | 051163-29A | 051163-29A | 2025-09-16 |
| 04048223129517 | SPROTTE® NRFit | 041163-29A | 041163-29A | 2025-09-16 |
| 04048223129647 | SPROTTE® | 071151-30C | 071151-30C | 2025-09-16 |
| 04048223129678 | SPROTTE® NRFit | 021163-30C | 021163-30C | 2025-09-16 |
| 04048223129692 | SPROTTE® NRFit | 031163-27A | 031163-27A | 2025-09-16 |
| 04048223129838 | SPROTTE® NRFit | 061163-29A | 061163-29A | 2025-09-16 |
| 04048223129999 | Standard Sprotte Needle | 321151-29A | 321151-29A | 2025-09-16 |
| 04048223131398 | Standard Sprotte Needle | 341151-31B | 341151-31B | 2025-09-16 |
| 04048223131428 | SPROTTE® | 131151-30C | 131151-30C | 2025-09-16 |
| 04048223131442 | SPROTTE® | 131151-30A | 131151-30A | 2025-09-16 |
| 04048223131466 | SPROTTE® | 141151-30C | 141151-30C | 2025-09-16 |
| 04048223132050 | SonoPlex® II Facet S | 001287-72 | 001287-72 | 2025-09-16 |
| 04048223132135 | SonoPlex® II Facet S | 001287-76 | 001287-76 | 2025-09-16 |
| 04048223132241 | SonoPlex® II Facet NRFit | 001265-74 | 001265-74 | 2025-09-16 |
| 04048223132319 | SonoPlex® II Facet NRFit | 001265-77 | 001265-77 | 2025-09-16 |
| 04048223132395 | SonoPlex® II Facet | 001285-76 | 001285-76 | 2025-09-16 |
| 04048223132463 | SonoBlock II Facet | 001280-74 | 001280-74 | 2025-09-16 |
| 04048223132562 | SonoPlex® II Facet S NRFit | 001267-76 | 001267-76 | 2025-09-16 |
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| 40888277832450 | MEDLINE INDUSTRIES, INC. | MEDLINE INDUSTRIES, INC. | BSP | 2025-12-18 |
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