Identity
- Trade Name
- PILLING FDA UDI
- Generic Name
- Aorta punch, single-use FDA UDI
- Device Name
- PUNCH DP-48K DISPOSABLE PUNCH 4.8 MILLIMETERS FDA UDI
- Model / Reference
- IPN011482 FDA UDI
- Description
- PUNCH DP-48K DISPOSABLE PUNCH 4.8 MILLIMETERS FDA UDI
Identifiers
- Catalog Number
- DP-48K FDA UDI
- Primary DI / UDI-DI
- 04026704410163 FDA UDI
- FDA Product Code
- DWS FDA UDI
- GMDN Term
- Aorta punch, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 870.4500 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
Yes
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
- Outer Diameter — 4.8 Millimeter FDA UDILength — 8 Inch FDA UDI
Category: Aorta punch, single-use
Pilling by Teleflex Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Aorta punch, single-use.
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- Aorta Punch 14 cm - 5 1/2" Ø 4.0 mm Stainless Steel — SURTEX INSTRUMENTS LTD · Class I
- SCANLAN® A/V Punch — SCANLAN INTERNATIONAL INC · Class I
- SCANLAN® A/V Punch — SCANLAN INTERNATIONAL INC · Class I
- SCANLAN® A/V Punch — SCANLAN INTERNATIONAL INC · Class I
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 I | Pending data |
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Manufacturer
- Manufacturer
- Teleflex Incorporated
Sources (1)
- FDA UDI fb92c05d-593a-4cb4-811d-0efb5132abcd 36 fields · synced May 30, 2026