Identity
- Trade Name
- WECK FDA UDI
- Generic Name
- Spring-loaded pneumoperitoneum needle, single-use FDA UDI
- Device Name
- WECKVISTA INSUFFLATION NEEDLE 14 GAUGE 120 MILLIMETER FDA UDI
- Model / Reference
- IPN914239 FDA UDI
- Description
- WECKVISTA INSUFFLATION NEEDLE 14 GAUGE 120 MILLIMETER FDA UDI
Identifiers
- Catalog Number
- 35120 FDA UDI
- Primary DI / UDI-DI
- 14026704644954 FDA UDI
- FDA Product Code
- HIF FDA UDI
- GMDN Term
- Spring-loaded pneumoperitoneum needle, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.1730 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 12 Centimeter FDA UDI
Category: Spring-loaded pneumoperitoneum needle, single-use
Weck by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Spring-loaded pneumoperitoneum needle, single-use.
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- Disposable insufflation-needle — Pajunk GmbH Medizintechnologie · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Teleflex Incorporated
Sources (1)
- FDA UDI 748d23a1-df5a-4bb2-aa4e-481b5a90ebc5 36 fields · synced May 30, 2026