Identity
- Trade Name
- Biopsy Punches, Sterile, 8.0 mm, Purple FDA UDI
- Generic Name
- Skin-coring punch, single-use FDA UDI
- Model / Reference
- 4096 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840117340923 FDA UDI
- FDA Product Code
- LRY 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
No
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Skin-coring punch, single-use
Biopsy Punches, Sterile, 8.0 mm, Purple by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Skin-coring punch, single-use.
- Integra® Miltex® — Integra LifeSciences Production Corporation · Class I
- Integra® Miltex® — Integra LifeSciences Production Corporation · Class I
- Thoratec® HeartMate 3™ — Thoratec Corp · Class III
- EDM3 — EDM 3, LLC · Class I
- SHARD — APPLIED DENTAL, INC. · Class I
- Integra® Miltex® — Integra LifeSciences Production Corporation · Class I
- EDM3 — EDM 3, LLC · Class I
- MedSource Skin Biopsy Punch — MEDSOURCE INTERNATIONAL LLC · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Dynarex Corp.
Sources (1)
- FDA UDI cd9357f5-f9b2-4220-b92e-4f9494981c79 32 fields · synced Jun 1, 2026