Identity
- Trade Name
- Centurion FDA UDI
- Generic Name
- Amniotic membrane perforator, single-use FDA UDI
- Device Name
- AMNIOTIC MEMBRANE PERFORATOR FDA UDI
- Model / Reference
- AM50A FDA UDI
- Description
- AMNIOTIC MEMBRANE PERFORATOR FDA UDI
Identifiers
- Catalog Number
- AM50A FDA UDI
- Primary DI / UDI-DI
- 00653160123364 FDA UDI
- FDA Product Code
- KDC FDA UDI
- GMDN Term
- Amniotic membrane perforator, 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
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
Category: Amniotic membrane perforator, single-use
Centurion by Centurion Medical Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Amniotic membrane perforator, single-use.
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- DeRoyal — DEROYAL INDUSTRIES, INC. · Class I
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class I
- BUSSE HOSPITAL DISPOSABLES — ROBERT BUSSE & CO., 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
- Centurion Medical Products
Sources (1)
- FDA UDI 5309be11-832b-4e89-ac9d-c5ea4fbeca41 35 fields · synced May 30, 2026