Identity
- Trade Name
- EDM3 FDA UDI
- Generic Name
- Skin-coring punch, single-use FDA UDI
- Device Name
- Biopsy Punches, sterile, 8.0 mm, purple. FDA UDI
- Model / Reference
- BP80 FDA UDI
- Description
- Biopsy Punches, sterile, 8.0 mm, purple. FDA UDI
Identifiers
- Catalog Number
- BP80 FDA UDI
- Primary DI / UDI-DI
- M202BP801 FDA UDI
- FDA Product Code
- MDM FDA UDI
- GMDN Term
- Skin-coring punch, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
No
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Skin-coring punch, single-use
Edm3 by Edm 3, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Skin-coring punch, single-use.
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- Acu-Punch — ACUDERM, 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
- Edm 3, Llc
Sources (1)
- FDA UDI 3dee0804-9552-4a25-a41f-a05cf82621ff 35 fields · synced May 31, 2026